Bioequivalence studies performed by Contract Research Organisation (Raptim Research Pvt. Ltd)

Bioequivalence studies performed by Contract Research Organisation (Raptim Research Pvt. Ltd)

This document is intended to communicate the South African Health Products Regulatory Authority’s (SAHPRA’s) position to all Applicants/ Holders of Certificates of Registration (HCRs) who intend to submit/ have submitted applications supported by bioequivalence studies conducted by Raptim Research Pvt. Ltd, a Contract Research Organisation (CRO) located in Mumbai, India. It also communicates SAHPRA’s intention to request information in terms of Section 19(2) of the Medicines and Related Substances Act, Act 101 of 1965, as amended (The Medicines Act).

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Document Number: CEM01-2026/27
Version: 1
Date Updated: 07/05/2026
File Type: www
Category: Communication to industry
Unit: CEM Pre-reg, Clinical Evaluations Management, General ECTD & human medicines