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Indian Government Eases Norms To Test & Launch Drugs

Indian Government Eases Norms To Test & Launch Drugs

In an attempt to ease norms for testing and introduction of new medicines in the country, the government has taken steps to fast-track approvals for clinical trials as well as launch of drugs already approved in other countries. Pharmaceutical companies planning to launch new drugs already approved outside India after conducting pre-clinical or toxicological studies on animals will not be required to repeat such studies in India for importing or manufacturing them here unless some specific concerns are raised, the Drugs Controller General of India, under the health ministry, said in a latest circular issued this week.

Niranjan Andhalkar

https://prorelixresearch.com/mr-niranjan-andhalkar/

He is the Director – Director – Strategic Management & Planning at ProRelix Research. His visionary leader with 17+ years of experience in clinical research, pharmaceuticals, CROs, and healthcare IT. Known for driving business growth, strategic collaborations, and innovation, he has successfully built and scaled organizations in the global clinical research ecosystem. With academic expertise in Biotechnology, Clinical Research, and an MBA in Operations Management, he combines scientific knowledge with strong business strategy to create impactful and sustainable healthcare ventures.

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prorelix research

ProRelix Research is the rapidly growing Contract/ Clinical Research Organization (CRO) with multi-country service capability supporting phase 1, 2, 3, & 4 clinical trials of Pharma, Biotech, Biopharma, Medical Device, Nutraceutical & Herbal companies to conduct in the USA, India, Europe & South East Asia.