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Regulatory Affairs

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Ensuring Regulatory Compliance

At RADICON'S ‘quality’ is the basic foundation on which products are developed and produced. At every stage of the production cycle, quality stems from strict adherence to GLP/cGMP requirements. Providing support are the latest international quality systems incorporated from concept to commercial production. The quality assurance team has developed systems to ensure that quality is built in to the process, leading to consistency of quality each time, every time.

Collaborating for Regulatory Excellence

The Regulatory Affairs department at RADICON'S is the vital link between the company and various health authorities for all regulatory related matters. Pharmaceutical Industry is one of the most regulated of all industries and therefore it is important for the Regulatory Affairs team to have a thorough understanding of pharmaceutical registration for each and every country. Data collected from the various other departments such as R & D, Manufacturing, Marketing etc, is assimilated and compiled for registering the company, products and for updating health authorities in various countries.