Procedure for Consultation Meetings with Clinical Trial Applicants

This document has been prep ared to serve as a guideline for applicants who wish to request a meeting with South African Health Products Regulatory Authority (SAHPRA). SAHPRA establish reserves the right to request any additional information to whether such meeting may be relevant as it is reliant upon a small group of high ly specialis ed ex be furnished to perts Guidelines and application forms are available from the office of the Chief Executive Officer and the SAHPRA website.