Regulatory Affairs

Expertise in eCTD file preparation for GCC- Bahrain, Kuwait, Oman, Qatar, Saudi Arabia, and the United Arab Emirates (UAE). CTD Compilation, ACTD Compilation, Medical Devices, Cosmetics, Personal care, Supplements, Veterinary, and Herbal products with authorities throughout the Globe. We are Contract Research Organization (CRO) that provides integrated services and consultancy to Pharmaceuticals, Biotechnology, Nutraceuticals, Herbal, Cosmetics and Medical devices companies. Regulatory professionals are responsible for: Keeping track of the ever-changing legislation in all the regions in which a company wishes to distribute its products. Advising on legal and scientific restraints and requirements. Collecting, collating and evaluating scientific data. Presenting registration...

Actd dossier,herbal & nutraceuticals dossier ,ectd dossier,ctd dossier,regulatory affairs,cosmetic dossier,food supplements,drug regulatory affairs,dmf,drug master files,cis countries,asian countries,african countries,third party manufacturing,tablets ,capsules,lozenges,injections,gcc ,dossier publishing ,regulatory guidelines,raps,and common technical documents

Regulatory affairs operates in the Pharmaceutical manufacturing industry.

Regulatory affairs's revenue is 11m - 100m

Regulatory affairs has 11 - 50 employees.