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The drug regulatory and clinical trials space is undergoing a major change in India. With an increasing buzz around health related issues and awareness levels going an all time high companies, government institutions and other major pharma corporate houses today are feeling the heat. What they need today is easy-to-access and ready-to-use regulatory information, schedules and compliance related information inputs. This information pertains to all kind of medical products viz., drug formulations, APIs, diagnostic kits, surgical and medical devices so that they can implement and execute their product development programmes in a timely fashion. We provide advisory services in regulatory areas to manufacturers, exporters, importers and contract manufacturers to one of the hottest areas facing the Indian pharma industry,namely fixed dose combinations.+ Read More
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