MIRA INFORM REPORT

 

 

Report Date :

15.12.2011

 

IDENTIFICATION DETAILS

 

Name :

GLENMARK PHARMACEUTICALS LIMITED

 

 

Registered Office :

B/2, Mahalaxmi Chambers, 22, Bhulabhai Desai Road, Mumbai – 400 026, Maharashtra

 

 

Country :

India

 

 

Financials (as on) :

31.03.2011

 

 

Date of Incorporation :

18.11.1977

 

 

Com. Reg. No.:

11-19982

 

 

Capital Investment / Paid-up Capital :

Rs.270.270 Millions

 

 

CIN No.:

[Company Identification No.]

L24299MH1977PLC019982

 

 

TAN No.:

[Tax Deduction & Collection Account No.]

MUMG07883B

 

 

Legal Form :

Public Limited Liability company. The company’s shares are listed on the Stock Exchanges.

 

 

Line of Business :

Manufacturing and Marketing of Pharmaceutical Products

 

 

No. of Employees :

7000 (Approximately)

 

 

RATING & COMMENTS

 

MIRA’s Rating :

Aa (74)

 

RATING

STATUS

 

PROPOSED CREDIT LINE

71-85

Aa

Possesses adequate working capital. No caution needed for credit transaction. It has above average (strong) capability for payment of interest and principal sums

Large

 

Maximum Credit Limit :

USD 79000000

 

 

Status :

Good

 

 

Payment Behaviour :

Regular

 

 

Litigation :

Clear

 

 

Comments :

Subject is a well established and reputed company having fine track. Financial position of the company appears to be sound. Fundamentals are strong and healthy. Trade relations are fair. Business is actives. Payments are reported to be regular and as per commitments.

 

The company can be considered normal for business dealings at usual trade terms and conditions.

 

NOTES :

Any query related to this report can be made on e-mail : infodept@mirainform.com while quoting report number, name and date.

 

ECGC Country Risk Classification List – September 30, 2011

 

Country Name

Previous Rating

(30.06.2011)

Current Rating

(30.09.2011)

India

A1

A1

 

Risk Category

ECGC Classification

Insignificant

 

A1

Low

 

A2

Moderate

 

B1

High

 

B2

Very High

 

C1

Restricted

 

C2

Off-credit

 

D


 

INFORMATION DECLINED BY

 

Name :

Mr. Aditya Parulakar

Designation :

Accountant

 

 

LOCATIONS

 

Registered / Administrative Office :

B/2, Mahalaxmi Chambers, 22, Bhulabhai Desai Road, Mumbai – 400 026, Maharashtra, India

Tel. No.:

91-22-24964893 / 24964894 / 24964895 / 24964896 / 56549999 / 55902491 / 92

Fax No.:

91-22-24932648 / 23512177 / 23519652

E-Mail :

glenmark@giasbm01.vsnl.net.in

webmaster@glenmarkpharma.com

Website :

http://www.glenmarkindia.com

http://www.glenmarkpharma.com

 

 

Corporate Office :

Gelnmark House, HDO – Corporate Building Wing A, B D Sawant Marg, Chakala, Off Western Express Highway, Andheri (East), Mumbai – 400 099, Maharashtra, India

Tel. No.:

91-22-40189999

Fax No.:

91-22-40189986

 

 

Manufacturing Facilities :

Formulations

 

·         E – 37, MIDC Industrial Area, D-Road, Satpur, Nasik – 422 007, Maharashtra, India

·         Plot No. 7, Colvale Industrial Estate, Bardez – 403 115, Goa, India

·         D-42, Plot No. 50, Kundaim Industrial Estate, Kundaim – 403 115, Goa, India

·         Village-Kishanpura, Baddi Nalagarh Road, Tehsil Nalagarh, District Solan, Baddi – 174 101, Himachal Pradesh, India

·         Business Unit II, Village Bhattanwala, PO Rajpura, Nalagarh District Solan, Himachal Pradesh, India

·         Plot No. 2, Phase-II, Pharma Zone, Special Economic Zone Area, Pitampur, Indore – 454 775, Madhya Pradesh, India

·         Rua Assahi, 33-1, Andar CEP: 09633-0110, Rudge Ramos Sao Bernardo Do Campo, Sao Paulo, Brazil

·         Rua Frei Liberato De Gries, 548, Jardim Arpoadar, CEP: 05572-210, Sao Paulo, Brazil

·         Glenmark Pharmaceuticals s.r.o., Fibichova 143, 56617, Vysoke Myto, Czech Republic

·         Calle 9 Ing Meyer Oks N 593, Parque Industrial Pilar, B1629MX Buenos Aires, Argentina 

 

API

 

·         3109-C, GIDC Industrial Estate, Ankleshwar, District Bharuch - 393 002, Gujarat, India

·         Plot No. 163-165/170-172, Chandramouli Industrial Estate, Mohal Bazarpeth, Sholapur – 413 213, Maharashtra, India

·         Plot No. A80, MIDC Area, Kurkumbh, Daund, Pune – 413 802, Maharashtra, India

 

 

 Manufacturing Facilities under Construction :

Formulations

·         Growth Centre, Samik-Marchak, District East Sikkim

 

API

·         Z-103 I, Dahej SEZ, Dahej District, Bharuch, Gujarat, India

·         Plot No. B-25, Five Star MIDC, Shendra District Aurangabad, Maharashtra, India

 

 

R and D Centers :

·         Plot No. A-607, TTC Industrial Area, MIDC, Mahape, Vashi, Navi Mumbai - 400 705, Maharashtra, India

·         Chemin de la Combeta 5, 2300 La Chaux-de-fonds, Switzerland

·         Plot No. C 152, MIDC Sinnar Industrial Area, Malegaon, District Nasik - 422 113, Maharashtra , India

·         Plot No. M4, Taloja Industrial Area, MIDC Taloja, Takula Panvel – 410 208, District – Raigad, Maharashtra, India

 

 

Clinical Research Centre :

·         Plot No. D 508, TTC Industrial Estate, MIDC, Turbhe, Navi Mumbai – 400 705, Maharashtra, India

·         C2 7600, The Quorum, Oxford Business Park, North Oxford, OX$ 2JZ, UK

 

 

Divisional Office :

Located at :- 

·         Mumbai

·         Delhi

·         Ghaziabad

·         Chennai

·         Bangalore

·         Hyderabad

·         Kolkata

·         Vadodara

·         Patna

 

 

Branch Office :

·         215/216, Adhyaru Industrial Estate, Sun Mill Compounds, Lower Parel, Mumbai – 400 013, Maharashtra, India

Tel. No. : 91-22-24982172

 

·         No. 2, Maharaja Surya Road, Alwarpet, Chennai – 600 018, Tamilnadu, India

·         Plot No. 39, Vasavinagar, Kharkana Main Road, Secunderabad–500 015, Andhra Pradesh, India

·         13-14-15, Bhargava Plaza, 4th N-Block, Rajaji Nagar, Dr. Rajkumar Road, Bangalore – 560 010, Karnataka, India

·         10/58, Kirth Nagar Industrial Area, New Delhi – 110 015, India

·         510, Commercial Point, 79, Lenin Sarani, Kolkata – 700 013, West Bengal, India

Tel. No. : 91-33-22449668 / 22467318

 

·         IBF Warehousing Complex, Meerut Road, Ghaziabad – 201 001, Uttar Pradesh, India

 

·         817-819, Sidharth Complex, R. C. Dutt Road, Alkapuri, Vadodara – 390 007, Gujarat, India

Tel. No. : 91-126-2337857 / 2342359

 

 

Overseas Office :

·         Glenmark Pharmaceutica LDA

Lote 4 – 2 – DT, Qta Do Meio, Rua Combatentes Do Ultramar, 2675 Odivelas, Portugal

 

·         Glenmark Pharmaceuticals (Canada) Limited

2798, Thamesgate Dr., Unit 4, Mississauga, Ontario, Canada L4T 1T9

 

 

DIRECTORS

 

As on 31.03.2011

 

Name :

Mr. Gracias Saldanha

Designation :

Founder and Chairman Emeritus

Address :

Flat No.2, Windemere Cooperative Housing Society Limited, 236-A, Byramji Jeejibhoy Road, Bandra (West), Mumbai - 400 050, Maharashtra, India

Date of Birth/Age :

73 Years

Qualification :

M.Sc. with Diploma in Management Studies

Experience :

39 Years

Date of Appointment :

10.05.2011

 

 

Name :

Mr. Glenn Saldanha

Designation

Chairman and Managing Director

Address

Ivorick Apartments, Flat No.32, Third Floor, St. Cyril Road, Opp. St. Andrew School Gate, Bandra (West), Mumbai - 400 050, Maharashtra, India

Date of Birth/Age :

41 Years

Qualification :

B. Pharma / M.B.A.

Date of Appointment :

10.05.2011

 

 

Name :

Mrs. Cheryl Pinto

Designation :

Executive Director

Address :

Flat No. 6, Windemere Cooperative Housing Society Limited, 236-A, Byramji Jeejibhoy Road, Bandra (West), Mumbai - 400 050, Maharashtra, India

Date of Birth/Age :

44 Years

Qualification :

Graduate in Pharmacy

Experience :

23 Years

Date of Appointment :

01.08.2000

 

 

Name

Mr. Abhinna Sundar Mohanty

Designation

Executive Director

Qualification :

M. Sc., In-charge of Domestic Formulations

Date of Appointment :

Upto 10.05.2011

 

 

Name

Mrs. B. E. Saldanha

Designation

Non Executive Director

Address

Flat No.2, Windemere Cooperative Housing Society Limited, 236-A, Byramji Jeejibhoy Road, Bandra (West), Mumbai - 400 050, Maharashtra, India

Date of Birth/Age :

71 Years

Qualification

B.Sc., B. Ed.

Date of Appointment

01.01.1982

 

 

Name :

Mr. Julio F. Ribeiro

Designation :

Non Executive Director

Address :

51, Sagar Tarang, Worli Seaface, Worli, Mumbai - 400 025, Maharashtra, India

Date of Birth/Age :

82 Years

Qualification :

Ex-IPS

 

 

Name :

Mr. N. B. Desai

Designation :

Non Executive Director

Date of Birth/Age :

84 Years

Experience :

47 Years  

 

 

Name :

Mr. Sridhar Gorthi

Designation :

Non Executive Director

Date of Birth/Age :

39 Years

Qualification :

B.A., L.L.B. (Hons.) from National Law School of India University

 

 

Name :

Mr. D. R. Mehta

Designation :

Non Executive Director

Date of Birth/Age :

74 Years

Qualification :

Graduated in Arts and Law

Experience :

41 Years

 

 

Name :

Mr. Hocine Sidi Said

Designation :

Non Executive Director

Date of Birth/Age :

46 Years

Qualification :

B.A. (International Marketing)  

Experience :

21 Years

 

 

KEY EXECUTIVES

 

Name :

Mr. Marshall Mendonza

Designation :

Company Secretary

 

 

Name :

Mr. Aditya Parulakar

Designation :

Accountant

 


 

MAJOR SHAREHOLDERS / SHAREHOLDING PATTERN

 

As on 30.09.2011

 

Category of Shareholders

No. of Shares

Percentage of Holding

(A) Shareholding of Promoter and Promoter Group

 

 

(1) Indian

 

 

Individuals / Hindu Undivided Family

2,335,309

0.86

Any Others (Specify)

128,241,936

47.43

Trusts

128,241,936

47.43

Sub Total

130,577,245

48.29

(2) Foreign

 

 

Total shareholding of Promoter and Promoter Group (A)

130,577,245

48.29

(B) Public Shareholding

 

 

(1) Institutions

 

 

Mutual Funds / UTI

6,659,220

2.46

Financial Institutions / Banks

10,752,573

3.98

Foreign Institutional Investors

88,089,894

32.58

Sub Total

105,501,687

39.02

(2) Non-Institutions

 

 

Bodies Corporate

5,119,854

1.89

Individuals

 

 

Individual shareholders holding nominal share capital up to Rs.0.100 million

18,492,593

6.84

Individual shareholders holding nominal share capital in excess of Rs.0.100 million

8,211,685

3.04

Any Others (Specify)

2,475,739

0.92

Directors & their Relatives & Friends

76,359

0.03

Hindu Undivided Families

589,036

0.22

Non Resident Indians

1,658,779

0.61

Trusts

10,054

-

Clearing Members

141,511

0.05

Sub Total

34,299,871

12.69

Total Public shareholding (B)

139,801,558

51.71

Total (A)+(B)

270,378,803

100.00

(C) Shares held by Custodians and against which Depository Receipts have been issued

-

-

(1) Promoter and Promoter Group

-

-

(2) Public

-

-

Sub Total

-

-

Total (A)+(B)+(C)

270,378,803

-

  


 

BUSINESS DETAILS

 

Line of Business :

Manufacturing and Marketing of Pharmaceutical Products

 

 

Products :

Item Code No.

Product Description

300480.00

Terbutaline Sulphate + Bromehexine Hydrochloride + Guaiphenesin

300490.99

Clotrimazole

300490.79

Telmisartan

 

PRODUCTION STATUS (As on 31.03.2011)

 

Particulars

 

Unit

Installed Capacity

Actual Production

Injections

 

Litres

-

150119

Liquid Orals

 

Litres

8553666

4825608

Lotions and externals

 

Litres

870025

686220

Ointments and Creams

 

Kgs.

1153500

731372

Solids and Powders

 

Kgs.

113000

286185

Tablets and Capsules

 

Nos.

1182950000

760097746

Aerosol Spray

 

Nos.

3000000

357213

Inhaler Capsules

 

Nos.

400000

198558

Others

 

--

--

60142

 

Notes:

 

·         The products of the Company are exempt from licencing procedures.

·         Installed capacity, being a technical matter, has not been verified by the auditors. However, the management has certified the same.

·         Actual production includes goods manufactured at third party manufacturing facilities on loan licence basis and at leased facilities.

 

GENERAL INFORMATION

 

No. of Employees :

7000 (Approximately)

 

 

Bankers :

Bank of India, Mahalaxmi Branch, Mumbai – 400 026, Maharashtra, India

 

 

Facilities :

Secured Loans

31.03.2011

Rs. In Millions

31.03.2010

Rs. In Millions

From Banks

 

 

Term Loan

223.400

338.550

Working Capital Facilities

1377.920

147.850

Total

1601.320

486.400

 

Notes:

 

1.       Term loan is secured by way of exclusive charge as the case may be, at certain locations, on Company's fixed assets both present and future.

 

2.       Working Capital Facilities is secured by hypothecation of Stocks of raw materials, packing materials, finished goods, work in process, receivables and equitable mortgage on fixed assets at the manufacturing facility at Nasik and Research and Development centre at Sinnar, Nasik both present and future. 

 

 

Unsecured Loans

31.03.2011

Rs. In Millions

31.03.2010

Rs. In Millions

Short Term Loan From Banks

6595.910

1221.730

Other Loans from Banks

3234.000

4481.730

Foreign Currency Convertible Bonds

0.000

1354.200

Security Deposit

31.230

53.490

Total

9861.140

7111.150

 

 

Banking Relations :

--

 

 

Auditors :

 

Name:

Walker, Chandiok and Company

Chartered Accountants

Address:

Mumbai

 

 

Cost Auditors:

 

Name:

Sevekari Khare and Associates

Chartered Accountants

Address:

Mumbai

 

 

Solicitor : 

  • Kanga and Company, Mumbai
  • Trilegal, Mumbai  

 

 

Subsidiaries Companies :

  • Glenmark Pharmaceuticals Europe Limited, U.K.
  • Glenmark Generics (Europe) Limited, U.K.
  • Glenmark Pharmaceuticals S.R.O., Czech Republic
  • Glenmark Pharmaceuticals SK, s.r.o., Slovak Republic
  • Glenmark Pharmaceuticals S. A., Switzerland
  • Glenmark Holding S. A., Switzerland
  • Glenmark Generics Holding S. A., Switzerland
  • Glenmark Generics Finance S. A., Switzerland
  • Glenmark Pharmaceuticals S.R.L., Romania
  • Glenmark Pharmaceuticals Eood., Bulgaria
  • Glenmark Distributor SP z.o.o., Poland
  • Glenmark Pharmaceuticals SP z.o.o., Poland
  • Glenmark Generics Inc., USA
  • Glenmark Therapeutics Inc., USA
  • Glenmark Farmaceutica Ltda., Brazil
  • Glenmark Generics SA., Argentina
  • Glenmark Pharmaceuticals Mexico, S.A. DE C.V., Mexico
  • Glenmark Pharmaceuticals Peru SAC., Peru
  • Glenmark Pharmaceuticals Colombia Ltda., Colombia
  • Glenmark Uruguay S.A., Uruguay
  • Glenmark Pharmaceuticals Venezuela., C.A , Venezuela
  • Glenmark Dominicana SRL, Dominican Republic
  • Glenmark Pharmaceuticals Egypt S.A.E., Egypt
  • Glenmark Pharmaceuticals FZE., United Arab Emirates
  • Glenmark Impex L.L.C., Russia
  • Glenmark Philippines Inc., Philippines
  • Glenmark Pharmaceuticals (Nigeria) Limited, Nigeria
  • Glenmark Pharmaceuticals Malaysia Sdn Bhd., Malaysia
  • Glenmark Pharmaceuticals (Australia) Pty Limited, Australia
  • Glenmark South Africa (Pty) Limited, South Africa
  • Glenmark Pharmaceuticals South Africa (Pty) Limited, South Africa
  • Glenmark Exports Limited, India
  • Glenmark Generics Limited, India
  • Glenmark Generics B.V., Netherlands
  • Glenmark Arzneimittel Gmbh., Germany

 

 

Joint Venture :

Glenmark Pharmaceuticals (Thailand) Company Limited, Thailand

 

 

CAPITAL STRUCTURE

 

As on 11.08.2011

 

Authorised Capital : Rs.750.000 Millions

 

Issued, Subscribed & Paid-up Capital : Rs.270.413 Millions

 

As on 31.03.2011

 

Authorised Capital :

No. of Shares

Type

Value

Amount

350000000

Equity Shares

Re.1/- each

Rs.350.000 Millions

4000000

Cumulative Redeemable Non-convertible

Preference Shares

Rs.100/- each

Rs.400.000 Millions

 

Total

 

Rs.750.000 Millions

 

Issued, Subscribed & Paid-up Capital :

No. of Shares

Type

Value

Amount

270272053

Equity Shares

Re.1/- each

Rs.270.270 Millions

 

Note

 

·         During the year ended 31st March, 2011 the Company, pursuant to Employee Stock Option Scheme 2003, has granted 227000 options at market price as defined in SEBI (ESOS) Guidelines and cancelled 488300 options.

 

·         During the year 434500 options were converted into Equity Shares under the Employee Stock Option Scheme, 2003. As at 31st March, 2011, 1937700 options were outstanding under Employee Stock Option Scheme 2003. On exercise of the options so granted under Employee Stock Option Scheme 2003, the paid-up Equity Share Capital of the Company will increase by a like number of shares.

 

·         On 18th September 2009, the Company allotted 18712935 Equity Shares of Re.1 each at a premium of Rs.220/- per share to Qualified Institutional Buyers pursuant to chapter VIII of the Securities Exchange Board of India (Issue of Capital and Disclosure Requirement) Regulation 2009.

 

·         Of the above 158371140 Equity Shares of Re.1 each are allotted as fully paid-up Bonus Shares by Capitalization of Reserves.

 


 

FINANCIAL DATA

[all figures are in Rupees Millions]

 

ABRIDGED BALANCE SHEET

 

SOURCES OF FUNDS

 

31.03.2011

31.03.2010

31.03.2009

SHAREHOLDERS FUNDS

 

 

 

1] Share Capital

270.270

269.840

250.520

2] Share Application Money

0.000

0.000

0.000

3] Reserves & Surplus

19527.140

17428.110

12049.185

4] (Accumulated Losses)

0.000

0.000

0.000

NETWORTH

19797.410

17697.950

12299.705

LOAN FUNDS

 

 

 

1] Secured Loans

1601.320

486.400

1122.123

2] Unsecured Loans

9861.140

7111.150

9536.950

TOTAL BORROWING

11462.460

7597.550

10659.073

DEFERRED TAX LIABILITIES

330.570

327.710

411.232

Foreign currency monetary item translation difference account 

0.000

36.210

0.000

 

 

 

 

TOTAL

31590.440

25659.420

23370.010

 

 

 

 

APPLICATION OF FUNDS

 

 

 

 

 

 

 

FIXED ASSETS [Net Block]

2237.790

1904.080

1728.069

Capital work-in-progress

399.430

468.830

324.493

 

 

 

 

INVESTMENT

10412.470

9929.200

2376.317

DEFERREX TAX ASSETS

101.270

96.730

88.060

 

 

 

 

CURRENT ASSETS, LOANS & ADVANCES

 

 

 

 

Inventories

1570.070
1503.980

1303.143

 

Sundry Debtors

1893.440
3300.920

4098.190

 

Cash & Bank Balances

309.490
50.770

116.877

 

Other Current Assets

0.000
0.000

0.000

 

Loans & Advances

16919.380
10511.140

15726.828

Total Current Assets

20692.380
15366.810

21245.038

Less : CURRENT LIABILITIES & PROVISIONS

 

 

 

 

Sundry Creditors

1344.020
791.800

1490.474

 

Other Current Liabilities

710.880
1118.610

742.081

 

Provisions

198.000
195.820

159.412

Total Current Liabilities

2252.900
2106.230

2391.967

Net Current Assets

18439.480
13260.580

18853.071

 

 

 

 

MISCELLANEOUS EXPENSES

0.000

0.000

0.000

 

 

 

 

TOTAL

31590.440

25659.420

23370.010

 

PROFIT & LOSS ACCOUNT

 

 

PARTICULARS

31.03.2011

31.03.2010

31.03.2009

 

SALES

 

 

 

 

 

Net Sales and Operating Income

11535.510

9830.280

8661.724

 

 

Other Income

314.720

91.900

994.923

 

 

TOTAL                                     (A)

11850.230

9922.180

9656.647

 

 

 

 

 

Less

EXPENSES

 

 

 

 

 

Cost of sales

3914.140

3263.930

3055.159

 

 

Selling and Operating Expenses

4288.090

4473.210

2880.774

 

 

Research and Development

Expenses

569.200

460.550

514.584

 

 

Exceptional Item

0.000

0.000

2.980

 

 

TOTAL                                     (B)

8771.430

8197.690

6453.497

 

 

 

 

 

Less

PROFIT BEFORE INTEREST, TAX, DEPRECIATION AND AMORTISATION (A-B)      (C)

3078.800

1724.490

3203.150

 

 

 

 

 

Less

INTEREST (NET)                                               (D)

360.820

301.580

551.386

 

 

 

 

 

 

PROFIT BEFORE TAX, DEPRECIATION AND AMORTISATION (C-D)                                       (E)

2717.980

1422.910

2651.764

 

 

 

 

 

Less/ Add

DEPRECIATION/ AMORTISATION                     (F)

209.880

212.780

191.045

 

 

 

 

 

 

PROFIT BEFORE TAX (E-F)                               (G)

2508.100

1210.130

2460.719

 

 

 

 

 

Less

TAX                                                                  (H)

386.320

(74.500)

281.456

 

 

 

 

 

 

PROFIT AFTER TAX (G-H)                                (I)

2121.780

1284.630

2179.263

 

 

 

 

 

Add

PREVIOUS YEARS’ BALANCE BROUGHT FORWARD

8511.120

7480.980

5636.879

 

 

 

 

 

Less

APPROPRIATIONS

 

 

 

 

 

Proposed Dividend on Equity Shares

108.110

107.940

100.208

 

 

Tax on Proposed Dividend on Equity Shares

17.960

17.930

17.030

 

 

Residual Dividend and Dividend Tax

0.500

0.160

0.000

 

 

Transfer to General Reserve

212.190

128.460

217.926

 

BALANCE CARRIED TO THE B/S

10294.140

8511.120

7480.978

 

 

 

 

 

 

EARNINGS IN FOREIGN CURRENCY

 

 

 

 

 

Export of goods calculated on FOB basis

3020.010

2649.150

2068.524

 

 

Guarantee Commission

11.210

26.060

29.135

 

 

Interest on loan to subsidiaries

308.040

278.250

136.067

 

TOTAL EARNINGS

3339.260

2953.460

2233.726

 

 

 

 

 

 

IMPORTS

 

 

 

 

 

Materials

158.840

150.440

114.254

 

 

Capital Goods

166.850

77.920

182.620

 

TOTAL IMPORTS

325.690

228.360

296.874

 

 

 

 

 

 

Earnings Per Share - Basic (Rs.)

7.86

4.93

8.72

 

Earnings Per Share - Diluted (Rs.)

7.85

4.92

8.54

 

QUARTERLY RESULTS

 

PARTICULARS

 

 

30.06.2011

30.09.2011

Type

 

1st Quarter

2nd Quarter

Net Sales

 

3270.880

3827.190 

Total Expenditure

 

2214.160

3427.720

PBIDT (Excl OI)

 

1056.720

399.470

Other Income

 

36.900

9.480

Operating Profit

 

1093.620

408.950

Interest

 

129.540

1.630

Exceptional Items

 

0.000

0.000

PBDT

 

964.080

407.320

Depreciation

 

49.670

51.690

Profit Before Tax

 

914.410

355.630

Tax

 

189.760

41.030

Provisions and contingencies

 

0.000

0.0000

Profit After Tax

 

724.650

314.600

Extraordinary Items

 

0.000

0.000

Prior Period Expenses

 

0.000

0.000

Other Adjustments

 

0.000

0.000

Net Profit

 

724.650

314.600

 

 KEY RATIOS

 

PARTICULARS

 

 

31.03.2011

31.03.2010

31.03.2009

PAT / Total Income

(%)

17.90
12.95
22.57

 

 

 
 
 

Net Profit Margin

(PBT/Sales)

(%)

21.74
12.31
28.41

 

 

 
 
 

Return on Total Assets

(PBT/Total Assets}

(%)

10.94
7.01
10.71

 

 

 
 
 

Return on Investment (ROI)

(PBT/Networth)

 

0.13
0.07
0.20

 

 

 
 
 

Debt Equity Ratio

(Total Liability/Networth)

 

0.69
0.55
1.06

 

 

 
 
 

Current Ratio

(Current Asset/Current Liability)

 

9.18
7.30
8.88

 

 

LOCAL AGENCY FURTHER INFORMATION

 

RESULTS OF OPERATIONS

 

On standalone basis the Company achieved a gross revenue of Rs.12122.480 millions and the Standalone operating profit before interest, depreciation and tax was Rs.3078.800 millions as compared to Rs.1724.490 millions in the previous year.

 

MANAGEMENT DISCUSSION AND ANALYSIS

 

GLOBAL ECONOMY OUTLOOK

 

Nearly four years after the onset of the largest financial crisis since the Great Depression, global financial stability is still not assured and significant policy challenges remain to be addressed. Even though global economic growth has accelerated, global financial stability has yet to be secured.

 

In advanced economies, activity has moderated less than expected, but growth remains subdued and unemployment is still high. The slow growth prospects and accommodative monetary policies of advanced economies, aided by relatively favorable fundamentals and carry trade opportunities in emerging market economies have spurred capital flows to such economies. This creates upward pressure on asset markets in receiving countries, while raising the latent risk that inflows could reverse and, as a result, poses considerable policy challenges on how best to absorb the flows. In many emerging economies, inflation pressures are also emerging, and there are now some signs of overheating, driven in part by strong capital inflows.

 

GLOBAL PHARMA SCENE

 

2011 marks the beginning of a critical two year period where global innovative pharma companies stand to lose the maximum value to generic competition due to high value patent expirations. The total value at risk stands at more than USD 30 Bn in 2011. This impending loss of value, aided by the lower new drug approval rates by major regulatory agencies including US FDA, increased costs of drug development and drying up of R and D pipelines, had spurred Big Pharma to adopt a battery of strategies in the past few years to minimize its effect and make avenues for future growth. The two major strategies that have emerged are as follows:

 

Pharmerging Markets: The hot spot of pharma action

 

As countries recover from the global economic crisis at different rates, there is growing divergence in the pace of pharmaceutical growth among major markets. While the emerging markets, or the Pharmerging markets, stand to benefit from greater government spending on healthcare and broader public and private healthcare funding, the advanced markets are expected to continue growing at much lower rates in FY 12. Pharmerging countries are forecast to grow at a 15-17 percent rate in 2011, to $170-180 billion, vis-a-vis the single digit growth rates expected for the developed markets.

 

The recent political developments in the Middle East also threatened to affect there covery of the global economy, specially the emerging economies like India, that rely on the Middle East for their oil requirements, by driving up inflation levels. But with Saudi Arabia stepping up to make up for war-torn Libya in terms of oil supply, the effect of the same has thus far been somewhat less pronounced.

A more influential crisis had been the one that hit the world’s 3rd largest economy. The earthquake and tsunami, followed by the nuclear emergency, have definitely been one of the worst crises that have hit Japan, and stand to have ripple effect across the global economy. The long-term effects of this event on the world economy shall be unfolding in the coming year.

 

Notwithstanding these factors, financial market performance has been favorable thus far in early 2011, reflecting the more positive economic climate, ample liquidity, and expanding risk appetite.

 

Although the growth prospects make these markets attractive avenues for future growth, multiple factors have made inroads into these markets relatively less easy.

 

Overpriced Valuations

 

A recent flurry of mergers and acquisitions in the Pharmerging space have driven up valuations of the local companies steeply, thus depriving Big Pharma of the option of good local acquisitions to quite an extent. However, the deep pockets and appetite for growth of these companies still promise a few high value deals in the Pharmerging markets in the near future.

 

Pricing Controls

Most markets, including the Pharmerging markets have continually beefed up their cost containment measures in the last few years. With the addition of more and more products into the list of price controlled products, companies will find it harder to derive good margins from their businesses.

 

Barriers to Entry

The influx of huge investment by MNC pharma companies into the Pharmerging markets also manifests into higher level of competition for the local players. With deeper pockets and better product portfolios, MNCs stand to take away huge chunks of business from these players. Hence, many governing bodies have started setting up direct/indirect barriers to entry to manage the direct and indirect impact of this keen interest of MNCs on the local players, as well as the final consumers. Insistence of local manufacturing of the products filed to enable faster approvals, governed prices and competition for IP protected products are just a few of the tools that governments have used to shield the local players and consumers

 

Biologics and Biosimilars: New Avenues for growth

The industry is slowly moving away from the primary care, small molecule driven sales model, towards targeting specialist secondary care indications through the use of high-value biologic therapies. Industry pundits predict that, by 2016, bio engine ered vaccines and biologics will account for 23 % of the global market (measured by value), up from 17 % in 2009. This is attributed to the high unmet need satisfied by these drugs, their high price points and the relative recent entry of many biologics into the market, hence ensuring protected value for some time. Also, bio similars that face patent expiry are largely insulated from sales erosion due to the high barriers to market entry at present.

 

But although the entry barriers are high, generic companies are not shying away from this opportunity. Increasingly the branded biologics face the threat of sales erosion from bio similars post-patent expiry, with the biosimilars market estimated to reach $76 billion through 2020. Approval pathways for bio similars have been set up in Europe and Japan, with bio similars already launched in both regions. US currently lags behind in this regard. However, intense debates are ongoing to finalize a pathway for the same.

 


BUSINESS REVIEW

 

During the financial year, the Specialty Business focused on 3 critical are as globally:

 

People Development

They have focused on enhancing the productivity of their most critical resource, their people. Their training and development efforts encompassed skill, personality, as well as leadership facets of their human capital, resulting in better performance of their people across the value chain.

 

Product Pipeline Management

Continuing with their therapeutic focus strategy, they have strived to bolster the portfolio of their key therapy areas, across markets. Their new product introduction process is now more robust, focusing on the quality of new launches, rather than the sheer number.

 

Operational Efficiency

During the year, the focus on improving operational efficiency was evident at all levels of the value chain. They streamlined their field force and aligned them with their therapeutic focus to enhance productivity. Greater control was exercised on their in-channel inventory, as well as receivables management. The Company also put up additional capacities and processes to infuse their manufacturing and supply chain with heightened levels of efficiencies. All these efforts have resulted in solid secondary sales growth, higher profitability and higher cash flows.

 

INDIA FORMULATIONS

 

Sales for the formulation business in India increased to Rs.8446.880 millions (USD 184.020 millions) for the financial year as compared to Rs.7528.620 millions in the previous corresponding year, recording a growth of 12 %.

 

The Company has registered value growth of 23.9 % vis-a-vis the industry growth of 15.3% (ORG: MAT Mar 2011) to attain 25th rank and gaining 0.10 % market share in FY 11 as per MAT Mar 2011. The growth is driven by significant gains in market share and rankings of top brands as per ORG (MAT Mar 2011).

 

·         Ascoril (Expectorant + Mucolytic) has gained 11 ranks to be at 91 (MAT Mar 2010ranked 102)

·         Telma (Telmisartan) gained 40 ranks to be at 95 (MAT Mar 2010 ranked 135)

·         Telma-H (Telmisartan, Hydrochlorothiazide) has gained 37 ranks to be at 158 (MATMar 2010 ranked 195)

·         Candid (Clotrimazole) has gained 20 ranks to be at 270 (MAT Mar 2010 ranked 290)

 

The Company strengthened its footing in various therapeutic segments by exhibiting growth in market share such as Cardiology 2.35 % (MAT MS Mar 2010 2.0 %), Dermatologist8.34 % (MAT MS Mar 2010 8.0 %), Respiratory 2.67 % (MAT MS Mar 2010 2.22 %) and Gynecology1.25 % (MAT MS Mar 2010 1.08 %).

 

The Company further strengthened its presence in the respiratory segment by launch of“ Glenmark-Respiratory Division”, offering an innovative product basket comprising of Metered Dose Inhalers (MDIs), Dry Powder Inhaler formulations (DPIs) and devices developed in-house, with a focus on better drug deposition and improved patient compliance. The Dry Powder Inhalation (DPI) formulation is based on patented PLATFORM technology.

 

The launch and implementation of Glenmark Focused Reporting for Complete Efficiency, or G Force last year started yielding its fruits, proving itself as an effective business intelligence tool for performance evaluation, tracking sales force activities and monitoring sales trend. Faster information flow through G Force significantly enhanced the productivity of sales team and further boosted sales performance efficiency byestablishing process driven sales management.

 

Glenmark has always been proactive in dissemination of scientific information and latest updates facilitating Doctor in their clinical practice. It took a step forward to establish a ‘Knowledge Point’ to address Medical Queries through MIDAS (Medical Information and Dissemination Services). MIDAS aims at providing quick response to any query or the latest information to doctors. The Company also implemented Webinar, at echnologically advanced module to reach doctors for conducting continuous medical education program. Webinar is an efficient model to address doctors across India at one instance, demonstrating product benefits and features, clinical evidences and addressing the queries of doctors by therapy leaders from medical fraternity.

 

ROW MARKETS

 

Russia CIS

 

During the entire financial year there was high focus on improving operational efficiency at all levels which resulted in solid secondary sales growth, higher profitability and higher positive net cash flow for the Russian operations. The Company showed a revenue growth of 45 % for the year. This significant increase in sales was backed by effective sales force activities and good growth in power brands. The new product - Glencet, launched at the end of Q3 FY 11 is gaining momentum and has shown a positive trend.

 

According to the latest Pharm expert data (Mar 2011) the Company has registered a value growth of 31.83 % vis-a-vis that of the industry 6.46 % (on a MAT basis). They are the fastest growing Indian company in Russia and Glenmark is now ranked 62 among the pharmaceutical companies in the country, gaining 11 ranks vis-a-vis March 2010. The market share across dermatology segment increased from 1.18 % to 1.56 %. Glenmark’s rank in the dermatology segment has gone up to 18 (MAT Mar 2011) gaining 6 ranks vis-a-vis March2011 (on a MAT basis).

 

The year gone by has also been one of the most dynamic on the regulatory front, with stricter and more elaborate clinical requirements for product registrations. This change has increased the bar for future product approvals of the pharma industry in Russia. To overcome these barriers in long-term, the Company has become more focused and prioritized its product development and filing efforts. The newly established Clinical Research Operations Group will also have a critical role in managing the clinical requirements for these products, while providing valuable cost efficiencies. The existing pipeline of products with the Russian FDA and the cosmeceutical range promises to support the buoyant growth numbers in short term.

 

In the other CIS markets, Ukraine, Kazakhstan and Uzbekistan are continuing to show positive trend in secondary sales. The Company is in the process of appointing national distributors in all these countries, which will ensure wider and faster availability of all its products and strengthen secondary sales for the units.

 

Africa and Middle East

 

Although the economies of Africa and Middle East region went through some turbulence in the year due to certain political developments, Glenmark’s Africa and Middle East operations continued to move against the winds with an impressive growth in overall sales. The focused and effective marketing and service, along with targeted product launches further enhanced the Company’s clout with the medical fraternity, manifesting in a secondary sales growth of 39 % over the previous year. The growth was driven by the performance of the key markets of South Africa, Sudan and Kenya, each of them showing more than 40 % growth in sales. Our Power and Focus brands strategy continued to yield fruits, with brands like Ascoril, Relcer and the Candid Range all registering double digit secondary sales growths.

The year was marked by several first-to-market innovative product launches across key therapeutic categories.

 

In the year, the Company also put in place various systems to enhance the control and service levels, as well as overall inventory and cash flow positions in the region.

 

Asia

 

The year has clearly been one of consolidation and growth for the Company’s Asia business. While the operations strived to strengthen its markets and instill efficiencies across the value delivery chain, significant efforts were undertaken on marketing front to strengthen relationship with Key Opinion Leaders (KOLs) and enhance the awareness and up take of its power and focus brands. The business showed a healthy secondary sales growth of 22 % over the previous year, driven majorly by some specific activities for building KOL relationships and improving value delivery efficiencies.

 

In its endeavor to strengthen the presence in key therapy segments of Dermatology and Internal Medicine, Glenmark convened two regional scientific forums: iLEAD

 

With the Middle East economies showing positive trends and various systems in place, the Company is confident of continuing with this healthy positive trend in the next year.

 

(International League of Experts for Advancement of Dermatology) and iLEAP (International League of Experts for Advancements of Physicians) in the year. iLead and iLeap are platforms where eminent KOLs from 6 different countries viz. Philippines, Malaysia, Vietnam, Sri Lanka, Myanmar and Cambodia come together and participate in interactive scientific sessions encompassed contemporary topics, latest clinical content published worldwide and clinical case discussions that provide food for thought and many take-home messages.

 

The strategy of Power and Focus brands continued to give rich dividends in Asia, contributing nearly 60 % of the overall sales. An important landmark for the year was the entry of Glenmark’s Vietnam operations into the lucrative hospital market of Vietnam. The Company also launched two specialized sales teams Cuticare and Respicare, in Philippines to further enhance its sales and marketing effectiveness.

 

In the year, Glenmark received 31 products approvals for the region, and did many high impact launches, including the launch of Deriva MS and Klenzit MS in Malaysia, Vietnam,

 

Latin America

 

Latin America continues to be a focus area for Glenmark. The revenue from the Latin American (Lat Am) and Caribbean operations was at Rs.1918.860 Millions (USD 41.80 Millions) for FY 11 as against Rs.1360.900 Millions (USD 28.50 Millions) a growth of 41 %.

 

Brazil remained the key country for the region, contributing to nearly 78 % of the overall turnover. The restructuring efforts put by the Company in FY 10 started to pay off in FY 11, with the secondary uptake showing a healthy increase over the previous year. A major growth driver for the Brazil operations this year has been the strengthening of Company’s oncology and dermatology portfolios by a mix of in-licensed and in-house product launches. There was an increased focus on maximizing field force productivity as well.

 

The year also saw an unequivocal focus on developing a stronghold in rest of the Latin American region, especially Mexico and Venezuela, the second and third largest pharmaceutical markets in Lat Am region. Albeit over a small base, the Upper Lat Amcountries doubled their secondary uptake vis-a-vis the previous year. This was majorly driven by the strong product pipeline and enhanced emphasis on improving field force productivity.

Central Eastern Europe

 

Relatively a new region for Glenmark, its Europe business has been growing at a steady rate. Glenmark Europe’s operations revenue for the entire financial year was Rs.1527.650 Millions (USD 33.28 Millions) as compared to  Rs.1362.750 Millions (USD 28.54 Millions) for the previous corresponding financial year, an increase of 12 %.

 

During the year, the Company’s aim was to fortify its position in current focus therapy areas, by the means of more efficient marketing efforts and high impact new launches that further strengthened its portfolio.

 

Through its marketing efforts, the Company strived to consolidate market shares of its existing products and gain share for the new ones. These efforts have manifested into many of its generic brands becoming the highest selling generics, even after relative late entry into the respective markets. The secondary sales for the entire region grew by 52 %for the year, vis-a-vis the market growth of 5 %, making Glenmark one of the fastest growing branded generic companies in the region.

 

Philippines and Sri Lanka, as well as the recent launch of Glemont (Monteleukast) in Malaysia in April 2011.

 

With robust systems in place, enhanced focus on generating maximum return on investment and new launches lined up, the Asia operations is all set to take a giant leap in the next year. dermatology portfolios across these markets by a mix of in-house development and in-licensing deals. The region sourced most of its oncology products from GGL’s Argentina plant, the Company’s hub for manufacturing and distribution of oncology products.

 

During the year, Venezuela also witnessed a significant devaluation of its currency. The Company was successful in minimizing its impact on its operations.

 

The Company also continued to focus on the search for new in-licensing opportunities and the launch of its own products under registration to scale up its European operations.

 

The year also saw the Company’s operations enter Latvia and Hungary. While Latviawas entered via a partner with the launch of two CNS and two cardiovascular products, Glenmark has appointed a distributor for its products in Hungary. It has also concluded the sales and marketing agreements Bulgaria and Portugal.

 

US Formulations

 

Glenmark Generics Inc., U.S.A. registered revenue from sale of finished dosage formulations of Rs.8351.560 Millions (USD 181.95 Millions) for FY 11 against revenue of Rs.7230.450 Millions (USD 151.440 Millions), an increase of 16 % in term over the previous year. It was a good year for Glenmark as it received the highest number of final ANDA approvals in the 2010calendar year from the U.S. FDA amongst all India-based manufacturers. It was also the only India-based generic company to receive final approval and launch a portfolio of oral contraceptive products in the U.S. market.

 

In the year, filed a total of 13 ANDAs with the FDA and was granted 22 ANDA approvals, comprised of 18 final and 4 tentative approvals. The Company aims to file another 20 ANDAs in the FY 12. The Company currently has 41 applications pending in various stages of the approval process with the US FDA. Also, the Company has 14 Para IV applications pendin gapproval of which Glenmark is the sole first-to-file for four products.

 

During the year, Glenmark, jointly with Lehigh Valley Technologies (LVT), received theapproval of two NDAs for a line of controlled substance products containing Oxycodone Hydrochloride by the US FDA. The two approved NDAs provide Glenmark and LVT with manufacturing and distribution rights to the only FDA-approved Oxycodone immediate release capsules and oral solution currently available in the United States and shall offset the loss of revenues due to withdrawal of Nitroglycerine tablets from the US markets due to a change in the governing rules for controlled substances.

 

Glenmark launched a total of 25 products during FY 11 comprised of a mix of immediate release tablets, extended release tablets, oral-contraceptives, semi-solid and controlled substance items. Glenmark’s marketing portfolio consists of 67 generic products authorized for distribution in the U.S. market.

 

During the first half of the fiscal year, Glenmark announced three settlements involving paragraph IV filings for atovaquone/proguanil tablets, ezetimibe tablets andeszopiclone tablets as follows:

 

·         Atovaquone/Proguanil tablets: Under the terms of the settlement agreement, Glenmark will be able to market and distribute its generic version of Malarone R tablets under a royalty-bearing license from GSK in the 3rd quarter of calendar year 2011, or earlier under certain circumstances.

·         Ezetimibe tablets: Glenmark will be able to its generic version of ZetiaR on December 12, 2016 or earlier under certain circumstances, ahead of the April 25, 2017expiration of Merck's patent exclusivity for Zetia R. Glenmark believes that it is entitled to 180 days of exclusivity as the first generic to file.

·         Eszopiclone tablets: Based on the terms of the settlement and license agreement, and upon approval, Glenmark would be permitted to launch its generic product on the later of November 30, 2013, or May 30, 2014 if Sepracor obtains paediatric exclusivity for Lunesta R. The settlement and license agreement and Consent Judgment and Order also would permit Glenmark to launch its generic product earlier under certain circumstances. Glenmark believes it is entitled to 180 days of exclusivity as the first generic to file.

 

During the year, Sanofi SA and Abbott Laboratories won a U.S. jury trial in which the drug makers sought to halt Glenmark’s sales of the generic version of their hypertension medicine Tarka. Abbott was awarded $16 million in damages. Although Glenmark was disappointed with the jury verdict, the judge has yet to consider Glenmark's defense that the patent is invalid for double patenting, to which the jury verdict is only advisory. Glenmark continues to believe that the patent is not valid.

 

Western Europe Formulations

 

Glenmark Generics continued to grow aggressively in Europe. Revenues for the full year of FY 11 were Rs.543.610 Millions (USD 11.840 Millions) against revenue of Rs.299.380 Millions (USD 6.270 Millions), ani ncrease of 82 %, in ` term, over the previous year.

 

As part of the strategy to expand the geographic footprint in Europe, the year saw the creation of two new subsidiaries in Western Europe. The European business now comprises Glenmark Generics (Europe) Limited is headquartered in UK and the new entities: Glenmark Generics B.V (GGBV) based in the Netherlands and Glenmark Arzneimittel GmbH (GAG) which is incorporated in Germany.

 

The business model for Glenmark Generics in Europe is built on creation of own businesses in a few selected key markets like the UK, Netherlands, Germany and the Nordic markets which follow the pure generic model, while licensing out to clients in several other EU markets on both a Pan-European as well as country specific basis. In markets where Glenmark is present through its entities (UK, Netherlands and Germany), the Company also seeks to add products through a selective in-licensing approach.

 

The UK business is currently the largest part of the EU business and this business continued to expand its coverage of the market by adding several new important accounts across both the wholesaling and retail channels and through new product launches which included in-house and in-licensed products. The sales and distribution infrastructure for the UK business is now well established and will grow significantly in the next year on the back of several new products which were in-licensed in this year.

 

GGBV won tenders for four products in the Netherlands and launched these on the Dutch market through contracts with several Health insurance companies. Glenmark follows a lean business model in the Netherlands which leverages on keeping low operating costs while maximizing on the business opportunity through tendered products. Glenmark Arzneimittel GmbH (GAG) was set up in Grobenzell near Munich and the Company laid the groundwork in order to procure local regulatory approvals for launching products in Germany in the next FY. GAG will actively target tender business in Germany while also promoting a few niche products through a non-tender route as part of its strategy to grow the business in Germany.

 

The out-licensing business made progress through the culmination of several new deals with Pan-European and local generic companies across the European markets. Through these deals, Glenmark currently supplies products to clients operating in 16 countries across Europe which include Austria, Germany, Spain, Finland, France, Greece, Hungary, Ireland, Italy, Netherlands, Poland, Portugal, Sweden, UK, Switzerland and Denmark.

 

GGEL in-licensed six new products and these are expected to be available for sales in UK for next financial year. On the regulatory front, the Company procured approval for its DCP procedures for At ovaquone-Proguanil and Mometasone cream and also submitted applications for Marketing authorizations through the DCP route for Desloratadine and Zolmitriptan ODT.

 

OUTLOOK

 

Glenmark's short-term and long-term outlook is encouraging for several reasons. On the discovery front, the pipeline is progressing well with 6 molecules in clinics, of which one is in Phase III and two in Phase II trials. The company will also continue with its approach of out-licensing its molecules. On the generics front, with high value patented drugs going off patent in the coming years, there is huge potential for the generics business. Glenmark is actively increasing its base in major generics markets of US and Western Europe.

 

CONTINGENT LIABILITIES AND CAPITAL COMMITMENT NOT PROVIDED FOR

 

Particulars

As on 31.03.2011

Rs. in millions

(a) Bank guarantees

20.280

Disputed income tax/excise duty/sales tax

27.370

Claims against the Company not acknowledged as debts (Refer Note i)

0.150

Open letters of credit

6.390

Indemnity bond

260.250

Call money payable to Glenmark Pharmaceuticals (Thailand ) Company Limited (16,415 shares @ THB 50 per ordinary share)

1.230

Corporate guarantee (Refer Note ii)

5687.130

Corporate guarantee (Refer Note iii)

1206.360

 

 

Note:

 

i) In respect of labour/industrial disputes

 

ii) Corporate guarantee given on behalf of various subsidiaries:

 

Citibank (Glenmark Holding SA, Switzerland (GHSA)

--

ICICI Bank (Glenmark Holding SA, Switzerland (GHSA))

638.920

Citibank (Glenmark Pharmaceuticals S.R.L Romania)

5.440

ALD Automotive (Glenmark Impex L.L.C., Russia)

102.410

ING Vysya Bank (Glenmark Generics Limited, India)

--

Central Bank of India (Glenmark Generics Limited, India)

1500.000

Citibank (Glenmark Farmaceutica Ltda, Brazil)

89.360

Yes Bank Ltd. (Glenmark Generics Limited, India)

--

Yes Bank Ltd. (Glenmark Generics Limited, India)

--

Citibank (Glenmark Impex L.L.C., Russia)

536.160

Citibank (Glenmark Impex L.L.C., Russia)

223.400

Citibank (Glenmark Pharmaceuticals SK s.r.o, Slovakia)

44.680

Citibank (Glenmark Pharmaceuticals S.R.L Romania)

134.040

Citibank (Glenmark Distributors SP z.o.o, Poland)

134.040

Citibank (Glenmark Impex L.L.C., Russia)

44.680

Citibank (Glenmark Holding S.A., Switzerland (GHSA))

2234.000

 

iii) The Company’s subsidiary, Glenmark Generics Inc., U.S.A (GGI) (formerly known as Glenmark Pharmaceuticals Inc., U.S.A. (GPI) on 2 June 2006 has entered into an Agreement with Paul Royalty Fund Holdings II (PRF) pursuant to which, PRF will pay upto USD 27 million to GGI for the development and commercialisation of certain products for the US market. Further, the Company has entered into a Master Services, License, Manufacturing and Supply Agreement with GGI to develop and manufacture the aforesaid products, and also issued a financial guarantee in favour of PRF for an amount not exceeding USD 27 million for the benefits under the said agreement.

 

(b) Estimated amount of contracts remaining to be executed on capital account, net of advances, not provided for

as at 31 March 2011 aggregate Rs.233.78 millions.

 

FIXED ASSETS

 

Tangible Assets

·        Freehold Land 

·         Leasehold Land

·        Factory Building

·        Other buildings and premises

·         Plant and Machinery

·         Furniture and Fittings

·         Equipments

·         Vehicles

 

Intangible Assets

·         Computer Software

·         Brands

 

WEB DETAILS

 

BUSINESS DESCRIPTION

 

Subject is a pharmaceutical company engaged in discovery of new molecules both new chemical entities (NCEs) and new biological entities (NBEs). The Company operates in five geographical areas: India, United States, Latin America, Europe and Rest of the World. Subject operates in three segments: specialty, generics and out-licensing. Specialty segment includes manufacture and distribution of branded products of subject. Specialty business is focused on range of therapeutic segments, such as dermatology, internal medicine, respiratory, pediatrics, diabetes, gynecology, oncology. Generics segment consists of finished pharmaceutical products ready for consumption by the patient, marketed under as generic finished dosages with therapeutic equivalence to branded formulations (generics). Out-licensing segment includes the discovery of new chemical entities for subsequent commercialization and out-licensing, as well as contract research services. For the nine months ended 31 December 2010, Subject’s revenues increased 24% to RS22.53B. Net income increased 65% to RS3.77B. Revenues reflect an increase in income from operations and higher other operating income. Net income also reflects a decrease in depreciation expenses and lower interest expenses. The Company is engaged in discovery of new molecules and is focused in the areas of inflammation and metabolic disorders.

 

BOARD OF DIRECTORS

 

Mr. Glenn Mario Saldanha - Executive Chairman of the Board, Chief Executive Officer, Managing Director

 

Mr. Glenn Mario Saldanha is Executive Chairman of the Board, Chief Executive Officer, Managing Director of subject. He is a B.Pharma from Bombay University and was awarded the Watumall Foundation Award for overall excellence. His other educational qualifications include an MBA from New York University’s Leonard N. Stern School of Business (US). He has worked for Eli Lilly in the US and was a Management Consultant with Price Waterhouse Coopers. His services have been used by Smithkline Beecham, Rhorer, Astra, Merck and Johnson and Johnson, among others.


Education

MBA , New York University

B , University of Bombay

 

Mr. Gracias A Saldanha - Non-Executive Chairman and Promoter

 

Mr. Gracias A. Saldanha is the Chairman Emeritus of subject effective from May 10, 2011. He is the fousnder of the Company. He has over 39 years experience in the industry. His educational qualifications include a M.Sc. from Bombay University with a Diploma in Management Studies from Jamnalal Bajaj Institute of Management Studies, Mumbai. He has worked with the pharmaceutical companies like Abbott Laboratories and E. Merck.


Education

MS , Bombay University

 

Mr. Natvarlal Bhimbhai Desai - Non-Executive Independent Director

 

Mr. Natvarlal Bhimbhai Desai is Non-Executive Independent Director of subject. He is a retired General Manager of Bank of Baroda. He has over 46 years experience in the Banking Sector. He has worked in India and overseas. He was Chairman of Bank of Baroda Uganda Limited.He was the founder and Managing Director of Equitorial Bank PLC, UK from which he retired in 1992.

 

Mr. Sridhar Gorthi - Non-Executive Independent Director

 

Mr. Sridhar Gorthi is Non-Executive Independent Director of subject. He is a B.A., L.L.B. (Hons.) from the National Law School of India University. Mr. Sridhar Gorthi is presently a partner in Trilegal and has worked with Arthur Anderson and Lex Inde, Mumbai. He is involved in legal advisory services to various multinational and domestic corporations on restructuring, debt finance, joint ventures, acquisition/mergers etc.


Education

LLB , National Law School of India University

BA , National Law School of India University

 


Mr. D. R Mehta - Non-Executive Director and Additional Director

 

Shri. Devendra Raj Mehta is the Non-Executive Independent Director of subject. He is a graduate in Arts and Law from Rajasthan University. He also studied at Royal Institute of Public Administration, London and the Alfred Sloan School of Management, Boston, USA. He has over 41 years experience in civil services and has held various positions in the Government of Rajasthan and Government of India. He was the Deputy Governor of Reserve Bank of India and also the Chairman of the Securities and Exchange Board of India (SEBI).


Education

LLB , Royal Institute of Public Administration

BA , Royal Institute of Public Administration

Management, Massachusetts Institute of Technology

 

Mr. Julio F. Ribeiro - Non-Executive Independent Director

 

Mr. Julio F. Ribeiro is Non-Executive Independent Director of subject. He is a retired government official and has served the country under various assignments. Amongst the positions held, he has been the Ex-Commissioner of Police, Mumbai, former Special Secretary to Government of India, Ministry of Home Affairs, former Director General of Police, Punjab, Ex-Adviser to the Governor of Punjab, Ex-Ambassador of India to Romania and is currently a Director in VVF Limited


Education

B Commerce, Bombay University

 

Mr. Hocine Sidi Said - Non-Executive Director

 

Mr. Hocine Sidi Said is the Non-Executive Independent Director of subject. He has graduated in B.A. (International Marketing). He is the Founder and Director of Bio-nAbler, an investment company that partners with Sovereign Wealth Funds and Private Equity Firms across Asia and the MENA region to identify and execute product and company acquisitions. He has over 21 years of experience in the pharmaceuticals industry and has worked with companies like Pfizer and UCB. During his stint at UCB, he was in charge of the entire Emerging Markets Region and designated as Senior Vice President. Prior to joining UCB, he spent close to 17 years with Pfizer in various senior management and developmental roles in the Middle East, Central and Eastern Europe and Asia.

 

Mrs. B. E Saldanha - Non-Executive Director and Promoter

 

Mrs. B. E. Saldanha is the Non-Executive Director of subject. She has graduated in B.Sc., B.Ed., from Bombay University and was a Whole-time Director of the Company from 1982 to 2005. She was responsible to an extent in developing the Company’s export business.


Education

B , University of Bombay

BS , University of Bombay

 


PRESS RELEASES

 

Glenmark Pharmaceuticals issues stock options

 

India, December 10 -- Glenmark Pharmaceuticals has informed that the compensation committee of the company, at its meeting held on December 07, 2011 has issued 25,000 stock options to permanent employees pursuant to ESOS 2003. Each option shall be convertible into one equity share of Re. 1 each in one or more tranches.The above information is part of the company's filing submitted to the BSE.

Outcome of Compensation Committee Meeting

 

India, December 09 -- Glenmark Pharmaceuticals Limited has informed BSE that the Compensation Committee of the Company, at its meeting held on December 07, 2011 has issued 25,000 stock options to permanent employees pursuant to ESOS 2003. Each option shall be convertible into one equity share of Re. 1/- each in one or more tranches.

 

Glenmark Pharmaceuticals Romania Eyes 25% Annual Sales Growth in Next Three Yrs

 

BUCHAREST (Romania), December 8 - The Romanian unit of Indian drug producer Glenmark Pharmaceuticals expects its sales to grow by more than 25% annually in the next three years, Bucharest-based media reported on Thursday.

 

The main driver of the growth expected in the next three years will be the launch of new products. Eighteen new products will be launched by the end of 2013," daily Ziarul Financiar (www.zf.ro) quoted the local unit's director general, Mariana Wencz, as saying.

 

Glenmark Pharmaceuticals Romania currently has 17 products in its portfolio.

 

The Romanian unit posted a turnover of 30 million lei ($9.3 million/7.0 million euro) in the fiscal year ended March 2011, Ziarul Financiar said.

 

Glenmark Pharmaceuticals' arm gets USFDA approval for Montelukast Sodium tablets

 

India, November 28 -- Glenmark Pharmaceuticals' - Glenmark Generics Incorporation, USA, (GGI) the US subsidiary of Glenmark Generics has been granted tentative approval from United States Food and Drug Administration (USFDA) for Montelukast Sodium 10 mg tablets, their generic version of Singulair tablets by Merck.IMS Health has recorded sales of Singulair 10 mg tablets for the 12 month period ending September 2011, as $3.2 billion. Based on the tentative approval for Montelukast Sodium tablets, Glenmark Generics should be able to launch the product upon patent expiry in August 2012.Singulair is indicated for the prophylaxis and chronic treatment of asthma in adults and pediatric patients 12 months of age and older, for prevention of exercise-induced bronchoconstriction (EIB) in patients 15 years of age and older, for the relief of symptoms of seasonal allergic rhinitis in patients 2 years of age and older and perennial allergic rhinitis in patients 6 months of age and older. Glenmark's current portfolio consists of 73 products authorized for distribution in the US marketplace. The company has over 40 ANDA's pending approval with the USFDA. In addition to these internal filings, GGI continues to identify and explore external development partnerships to supplement and accelerate the growth of the existing pipeline and portfolio. Glenmark Generics (GGL) is a subsidiary of Glenmark Pharmaceuticals (Glenmark) and aims to be a global integrated Generic and API leader. GGL has an established presence in North America, a developing EU presence and Argentina and maintains marketing front-ends in these countries. Glenmark Pharmaceuticals, a leader among the emerging market companies in drug discovery and development and most of its active substances in the pipeline are first-in-Class. Glenmark's achievements over the year include a major deal with Sanofi in Crohn's disease, completing Phase II trials of its first novel product, crofelemer and demonstrated higher sales and profit growth.

 


 

CMT REPORT (Corruption, Money Laundering & Terrorism]

 

The Public Notice information has been collected from various sources including but not limited to: The Courts, India Prisons Service, Interpol, etc.

 

1]         INFORMATION ON DESIGNATED PARTY

No records exist designating subject or any of its beneficial owners, controlling shareholders or senior officers as terrorist or terrorist organization or whom notice had been received that all financial transactions involving their assets have been blocked or convicted, found guilty or against whom a judgement or order had been entered in a proceedings for violating money-laundering, anti-corruption or bribery or international economic or anti-terrorism sanction laws or whose assets were seized, blocked, frozen or ordered forfeited for violation of money laundering or international anti-terrorism laws.

 

2]         Court Declaration :

No records exist to suggest that subject is or was the subject of any formal or informal allegations, prosecutions or other official proceeding for making any prohibited payments or other improper payments to government officials for engaging in prohibited transactions or with designated parties.

 

3]         Asset Declaration :

No records exist to suggest that the property or assets of the subject are derived from criminal conduct or a prohibited transaction.

 

4]         Record on Financial Crime :

            Charges or conviction registered against subject:                                                              None

 

5]         Records on Violation of Anti-Corruption Laws :

            Charges or investigation registered against subject:                                                          None

 

6]         Records on Int’l Anti-Money Laundering Laws/Standards :

            Charges or investigation registered against subject:                                                          None

 

7]         Criminal Records

No available information exist that suggest that subject or any of its principals have been formally charged or convicted by a competent governmental authority for any financial crime or under any formal investigation by a competent government authority for any violation of anti-corruption laws or international anti-money laundering laws or standard.

 

8]         Affiliation with Government :

No record exists to suggest that any director or indirect owners, controlling shareholders, director, officer or employee of the company is a government official or a family member or close business associate of a Government official.

 

9]         Compensation Package :

Our market survey revealed that the amount of compensation sought by the subject is fair and reasonable and comparable to compensation paid to others for similar services.

 

10]        Press Report :

            No press reports / filings exists on the subject.

 


 

CORPORATE GOVERNANCE

 

MIRA INFORM as part of its Due Diligence do provide comments on Corporate Governance to identify management and governance. These factors often have been predictive and in some cases have created vulnerabilities to credit deterioration.

 

Our Governance Assessment focuses principally on the interactions between a company’s management, its Board of Directors, Shareholders and other financial stakeholders.

 

 

CONTRAVENTION

 

Subject is not known to have contravened any existing local laws, regulations or policies that prohibit, restrict or otherwise affect the terms and conditions that could be included in the agreement with the subject.

 

 

FOREIGN EXCHANGE RATES

 

Currency

Unit

Indian Rupees

US Dollar

1

Rs.53.57

UK Pound

1

Rs.82.97

Euro

1

Rs.69.89

 


 

SCORE & RATING EXPLANATIONS

 

SCORE FACTORS

 

RANGE

POINTS

HISTORY

1~10

6

PAID-UP CAPITAL

1~10

8

OPERATING SCALE

1~10

8

FINANCIAL CONDITION

 

 

--BUSINESS SCALE

1~10

9

--PROFITABILIRY

1~10

9

--LIQUIDITY

1~10

9

--LEVERAGE

1~10

8

--RESERVES

1~10

9

--CREDIT LINES

1~10

8

--MARGINS

-5~5

--

DEMERIT POINTS

 

 

--BANK CHARGES

YES/NO

YES

--LITIGATION

YES/NO

NO

--OTHER ADVERSE INFORMATION

YES/NO

NO

MERIT POINTS

 

 

--SOLE DISTRIBUTORSHIP

YES/NO

NO

--EXPORT ACTIVITIES

YES/NO

YES

--AFFILIATION

YES/NO

YES

--LISTED

YES/NO

YES

--OTHER MERIT FACTORS

YES/NO

YES

TOTAL

 

74

 

This score serves as a reference to assess SC’s credit risk and to set the amount of credit to be extended. It is calculated from a composite of weighted scores obtained from each of the major sections of this report. The assessed factors and their relative weights (as indicated through %) are as follows:

 

Financial condition (40%)            Ownership background (20%)                 Payment record (10%)

Credit history (10%)                    Market trend (10%)                                Operational size (10%)

 


 

RATING EXPLANATIONS

 

 

RATING

STATUS

 

 

PROPOSED CREDIT LINE

>86

Aaa

Possesses an extremely sound financial base with the strongest capability for timely payment of interest and principal sums

 

Unlimited

71-85

Aa

Possesses adequate working capital. No caution needed for credit transaction. It has above average (strong) capability for payment of interest and principal sums

 

Large

56-70

A

Financial & operational base are regarded healthy. General unfavourable factors will not cause fatal effect. Satisfactory capability for payment of interest and principal sums

 

Fairly Large

41-55

Ba

Overall operation is considered normal. Capable to meet normal commitments.

 

Satisfactory

26-40

B

Capability to overcome financial difficulties seems comparatively below average.

 

Small

11-25

Ca

Adverse factors are apparent. Repayment of interest and principal sums in default or expected to be in default upon maturity

 

Limited with full security

<10

C

Absolute credit risk exists. Caution needed to be exercised

 

 

Credit not recommended

-

NB

                                       New Business

-

 

 

PRIVATE & CONFIDENTIAL : This information is provided to you at your request, you having employed MIPL for such purpose. You will use the information as aid only in determining the propriety of giving credit and generally as an aid to your business and for no other purpose. You will hold the information in strict confidence, and shall not reveal it or make it known to the subject persons, firms or corporations or to any other. MIPL does not warrant the correctness of the information as you hold it free of any liability whatsoever. You will be liable to and indemnify MIPL for any loss, damage or expense, occasioned by your breach or non observance of any one, or more of these conditions

This report is issued at your request without any risk and responsibility on the part of MIRA INFORM PRIVATE LIMITED (MIPL) or its officials.