Welcome to Sai Pharma Consultants

SaiPharma Regulatory Consultants are India based Pharmaceutical Regulatory consultant, Located in, Hyderabad, Telangana India. SaiPharma regulatory consultants are involved in a wide variety of regulatory consulting assignments for Regulated markets e.g. U.S.A, Europe, Canada, Australia etc. and Less regulated markets e.g. India, Asia Pacific, CIS, Middle- East, Africa etc. We have a team of experienced professionals, who driven by a hands-on work ethic, and were unencumbered by the administrative processes of a larger company. SaiPharma delivers higher quality regulatory documents in cost-effective manner.

Our Services

Drug Master File (US DMF)
Certificate of Suitability (CEP)
European DMF (EDMF)
Asian CTD (ACTD)
Training
Gap analysis
Query management
Amendments

SaiPharma regulatory consultant assist clients by guiding the product development in line with the country specific requirements, data generation, document compilation for submission to various Regulatory Agencies all over the world, responding to the queries and finally obtaining the approval or registration of the product.