Deep Manufacturing Expertise
We have 16 world-class manufacturing facilities of which 9 have a long history of regular USFDA inspections. With an annual capacity of nine billion tablets/ capsules a year, dedicated to servicing the more regulated markets, one of our finished dosages facilities is among the largest in Asia. Our facilities are designed to respond to a wide range of technologies - oral solids, injectibles, topicals, inhalers, cytotoxic, hormonals and other dosage forms.
Likewise our API facilities offer lean manufacturing, adhere to stringent regulatory guidelines and continually drive cost competitiveness. Such manufacturing capabilities and our inherent expertise to navigate intellectual property road blocks make us a preferred partner for some of the world’s leading pharmaceutical companies.
Globally Synchronized Supply Chain
We put the needs of our partners and customers first. Our globally synchronized supply chain and a comprehensive Information technology platform help us assure customers of timely delivery and superior inventory turns. The uninterrupted success of our customers’ business is our promise.
Regulatory Performance
Over the years we have built an expertise in understanding the regulatory frameworks of the various countries in which we operate. This has given us a distinctive edge, for ourselves and our customers. We have built a successful track record of timely and extensive approvals. As an example, we are among the leaders in terms of DMFs and ANDAs in the US itself, with more than half of these being Para IV possibilities.
Quality & Product Responsibility
At Dr Reddy’s, we strictly follow quality control and quality assurance systems as specified by regulatory requirements in each of the geographies in which we operate. For us, product responsibility extends through the life cycle of the product -- from product development to manufacture to product release to post-launch. We comply with the internationally accepted International Conference on Harmonization (ICH) guidelines in product development and we have independent quality control and quality assurance teams to ensure multi-stage quality compliance.
We have 16 world-class manufacturing facilities of which 9 have a long history of regular USFDA inspections. With an annual capacity of nine billion tablets/ capsules a year, dedicated to servicing the more regulated markets, one of our finished dosages facilities is among the largest in Asia. Our facilities are designed to respond to a wide range of technologies - oral solids, injectibles, topicals, inhalers, cytotoxic, hormonals and other dosage forms.
Likewise our API facilities offer lean manufacturing, adhere to stringent regulatory guidelines and continually drive cost competitiveness. Such manufacturing capabilities and our inherent expertise to navigate intellectual property road blocks make us a preferred partner for some of the world’s leading pharmaceutical companies.
Globally Synchronized Supply Chain
We put the needs of our partners and customers first. Our globally synchronized supply chain and a comprehensive Information technology platform help us assure customers of timely delivery and superior inventory turns. The uninterrupted success of our customers’ business is our promise.
Regulatory Performance
Over the years we have built an expertise in understanding the regulatory frameworks of the various countries in which we operate. This has given us a distinctive edge, for ourselves and our customers. We have built a successful track record of timely and extensive approvals. As an example, we are among the leaders in terms of DMFs and ANDAs in the US itself, with more than half of these being Para IV possibilities.
Quality & Product Responsibility
At Dr Reddy’s, we strictly follow quality control and quality assurance systems as specified by regulatory requirements in each of the geographies in which we operate. For us, product responsibility extends through the life cycle of the product -- from product development to manufacture to product release to post-launch. We comply with the internationally accepted International Conference on Harmonization (ICH) guidelines in product development and we have independent quality control and quality assurance teams to ensure multi-stage quality compliance.
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