RGI team has designed regular and value added services for importers and overseas brands looking to place their products in the Indian markets and provides exhaustive regulatory services for registrations, Manufacturing and marketing of drugs , cosmetics , Medical Devices and API.
Registration of IND’s, subsequent new drug and All categories of FDCs and as per the new drugs and Clinical Trials Rules 2019. Our team of professionals strives to ensure that all registrations are made efficiently and accurately, so that our customers always receive the best results.
We help our clients in arranging the CRO for BE and CT studies and obtaining the BE NOC, CT NOC and presenting the proposal to Subject Expert committee.
Thus, our expertise and experience in the CDSCO (India) process makes us a reliable choice for our customers.
We provide valuable support and expertise in
navigating the regulatory landscape, market entry strategies, quality management systems, Manufacturing infrastructure, Product Development, Technology transfer, Clinical Trials of MD and DPR for overall business development
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