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Sun Pharma






                          We were pioneers among Indian pharmaceutical companies to see
                          tremendous value in investing in research & development (R&D). Our
                          early investments in R&D, beginning three decades ago, enabled us to
                          make technology our key differentiator and develop a basket of robust
                          products for diverse markets across the world. Our core strength lies in
                          our ability to excel in developing generics and technologically complex
                          products through focused teams in formulations, process chemistry and
                          analytical development. We have the capability to deliver quality products
                          within established timelines, at low costs and without compromising on
                          quality.


                          We have around 2000 research scientists working in multiple R&D
                          centres equipped with cutting-edge enabling technologies for research.
                          Our scientists have expertise in developing generics, difficult to make
                          technology intensive products, Active Pharmaceutical Ingredients (APIs),
                          Novel Drug Delivery Systems (NDDS) and New Chemical Entities (NCEs).


                          Our capabilities span the development of differentiated products, such
                          as liposomal products, inhalers, lyophilised injections, nasal sprays,
                          besides developing controlled release dosage forms.
                          Over the years, we have developed expertise and gathered experience in
                          performing pharmacokinetic and bioequivalence studies to facilitate the
                          introduction of generic or branded generic drugs into the international
                          market. Our 408-bed clinical pharmacology unit with expert staff works
                          on bioequivalence/bioavailability studies in compliance with GCP.
                          Facilities include a full-fledged site for Phase I clinical studies. Our CPU
                          has been audited by US FDA, ANVISA, MHRA, and DCGI among others.
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