The depth of experience, capabilities, knowledge of our technical professionals and the strong scientific data make us expertise to compile CTD Files in line with International requirements, as well as in specific patterns requested by the MOH.

Our regulatory team consists of pharmacists and technical people proficient in:

• Preparing the CTD/ ACTD File/product dossiers as per the MOH guidelines
• Co-ordinating with the FDA & WHO agency for various certifications
• Legalization of the documents with the Embassies
• Resolving any technical queries with authentic in-depth data.