About Us

Regulatory Services India (RSI) is a leading regulatory consultancy in India, with over 10 years of experience in helping medical devices, IVD and Cosmetics companies from across the globe register their products with the Central Drugs Standard Control Organization (CDSCO), Ministry of Health and Family Welfare, Government of India.

We are a team of regulatory experts who have worked extensively with multinational companies as well as Indian Pharmaceutical Companies in a continuously evolving background of the Indian Regulations.

Our team can help you not only develop an optimal regulatory strategy for your product but also help register them with the Central Licensing authority in India.

With RSI, you get the assurance of a hassle-free journey to start marketing your medical devices in the exciting Indian market promising a high growth.

Regulatory Solutions India .

Seema Dutt

B.Pharm & M.Pharm from Mumbai University with 20+ years working with the Medical device and Pharmaceutical industry in the areas of regulatory affairs, quality assurance, clinical trial coordination, pharmacovigilance and technical documentation. Prior to 2011, she worked with organisations like Pharmacia Upjohn, Johnson & Johnson and Bausch & Lomb. She has solid knowledge of current Indian regulations, regulatory compliance, quality systems in Manufacturing/Warehousing & Distribution, Good Clinical Practices & ISO standards

Maneesh Dutt

B.Tech (Chemical Engineering) from IIT-D and MBA from ENI University, Milan with 25 years experience in various organisations (L&T, Reckitt & Coleman, STMicro). He complements the Regulatory functions of RSI bringing in strong strategy, project management & IP skills to the table. He is also the author of several best-selling management books. In the past, he also been associated with organisations across sectors as a consultant and trainer.
Ensure seamless market entry for your products. Contact us for expert regulatory support today!
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