This document has been prepared as a guide to assist applicants to comply with the requirements for Site Master Files with regard to all sites for pharmaceutical business....
This document has been prepared to serve as a recommendation to applicants wishing to conduct business as medicine wholesalers....
The objective of this procedure is to define the process to be followed and to provide instruction to the Holder of the Certificate of Registration (HCR) when submitting an application for Post-Importation Testing Exemption or imported products. ...
This document provides guidelines for the requirements of Good Manufacturing Practice (GMP) in South Africa. This guideline is not an exclusive approach. SAHPRA reserves the right to request any additional information to establish the safety, quality and efficacy of a medicine. SAHPRA may amend this...
