Glenmark
Glenmark
Glenmark
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SUMMARY OF BUSINESS<br />
Overview<br />
We are a research oriented, integrated pharmaceutical company incorporated in the Republic of India, with<br />
a presence in numerous markets around the world. We operate a specialty/proprietary business (“Specialty<br />
Business”) which is focused on drug development and branded generic drugs and a pure generics business<br />
(“Generics Business”) which operates in the unbranded generic drug market and the active pharmaceutical<br />
ingredients (“APIs”) market (each as more fully described below). We offer a range of products across<br />
various therapeutic segments including dermatology, gynaecology, oncology, diabetes, pain management<br />
and cardiovascular disease.<br />
We were incorporated in India on November 18, 1977 and became a public limited company on May 20,<br />
1996.<br />
Our Specialty Business is operated through the Company and focuses on new drug development and<br />
marketing of branded products. It is actively engaged in the development of new chemical entities<br />
(“NCEs”) and new biological entities (“NBEs”) and to out-licence them at appropriate junctures. To this<br />
effect, we have four research and development (“R&D”) centres, dedicated to the discovery and<br />
development of NCEs and NBEs. As at March 31, 2009, we had successfully out-licenced three molecules<br />
to four partners and had received a total of U.S.$117 million in up-front and milestone payments. Since<br />
March 31, 2009 two of the four out-licencing agreements have been terminated. We have established<br />
branded products in, niche therapeutic segments including dermatology, gynaecology, diabetes, pain<br />
management and cardiovascular diseases. We recognise the value of investing in original research in order<br />
to generate intellectual property assets that will sustain our revenues and earnings in a product patent<br />
regime post the General Agreement for Trade and Tariffs. We believe that these intellectual property assets<br />
allow us to establish our brands in regulated international markets and facilitate our growth as a global<br />
company. Towards this end, we have invested steadily in building a pipeline of NCEs, new NBEs and<br />
platform technologies. Currently, we have a pipeline of seven NCEs and two NBE in various phases of<br />
development.<br />
Within our Specialty Business, we operate a “branded generics” model. Our branded generics operations<br />
focus on the sale of our own branded, off-patent drugs. Important aspects of this business include brand<br />
building and prescription generation by way of marketing. We have a history of in-house brand<br />
development and, since incorporation, we have continued to launch new products at regular intervals. We<br />
first entered the dermatology market with the introduction of Candid Cream in 1979. We subsequently<br />
broadened our product range by introducing Candid–brand extensions in other therapeutic segments. In<br />
1987, we launched Ascoril, a cough expectorant. Our products Candid B, Ascoril, Telma and Telma H are<br />
among our successful brands, ranked 106, 127, 140 and 204 respectively among the top 300 brands as of<br />
July 2009. (Source: ORG IMS Health Incorporated SSA July 2009).<br />
Our Generics Business, operated through GGL, focuses on the generic drug markets in the United States of<br />
America (“United States”), parts of Europe and parts of Latin America, and on marketing and distribution<br />
of generic formulations and APIs. APIs are the principal ingredients for finished dosages and are also<br />
known as bulk actives or bulk drugs. APIs become formulations when the dosage is prepared for human<br />
consumption using additional inactive ingredients either in oral forms such as tablets, capsules, dry syrups<br />
or liquid orals or in sterile forms like injectable dry powder vials or liquid injectables. As of June 30, 2009,<br />
we have launched over 45 products in the United States generics market and have a further 45 abbreviated<br />
new drug applications (“ANDAs”) pending approval. We also generated, in October 2008, our first sales in<br />
the United Kingdom – through sales of Perindopril tablets. In addition, we sell APIs in over 70 countries.<br />
The Company has 33 subsidiaries, of which 32 are wholly-owned subsidiaries and, on a consolidated basis,<br />
we have, globally, more than 5,500 employees, over 25 representative offices and 12 manufacturing<br />
locations. We have over 2000 medical representatives located throughout India to market our products. We<br />
have established subsidiaries in Romania (<strong>Glenmark</strong> Pharmaceuticals s.r.l) and Poland (<strong>Glenmark</strong><br />
Pharmaceuticals Sp. zo.o and <strong>Glenmark</strong> Distributors Sp. zo.o) and have established a presence in numerous<br />
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