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The depth of experience, capabilities, knowledge of our technical professionals and the strong scientific data makes us expertised to compile Drug Master files in line with International requirements, as well as in specific patterns requested by the MOH.
This team consists of pharmacists and technical people proficient in :
Today, SGPharma holds many product registration in developing and advanced western countries across the world and new registrations are continuously added to the list.
Our vast experience in various markets and readily available Registration Dossiers, makes a fast turnaround time to start the business.
Studying registration guidelines
Preparing the Drug Master File/product dossiers as per the MOH guidelines
Co-ordinating with the FDA & WHO agency for various certifications
Conducting Bio-equivalence studies
Legalization of the documents with the Embassies
Resolving any technical queries with authentic in-depth data's