Regulatory Affairs

Supriya Lifescience Ltd. is committed to manufacture products in total compliance with regulatory requirements and customer expectations. All processes and manufacturing operations are in accordance with cGMP requirements, ICH guidelines and regulations, and in accordance with various health regulatory authorities like USFDA, EDQM, NMPA etc.

We are registered in more than 35 countries, and our facility has been audited by major health regulatory agencies. Our customers include innovator companies, big generic companies as well as several well-known Multi-National Corporations. We have filed 14 active USDMFs, 8 active CEPs and many more with various health authorities in Canada, Japan, South Korea, China and Australia.