Archive
17 Jul Process Flow of Importation of Medical Products Published
Posted at 13:50h
in
Please be informed that all documents and queries for GMP and CPP certificates should now be emailed to a new dedicated email address - see download. ...
27 Jul Guideline For Cultivation Of Cannabis
Posted at 16:54h
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This document provides the principles behind the minimum requirements in terms of quality, security and standard operating procedures relating to the cultivation of Cannabis and the manufacture and use of Cannabis-related pharmaceutical products for medicinal and research purposes that will need to be in place...
14 Jul Cannabis and related substances
Posted at 15:23h
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What is Cannabis?
Cannabis refers to the plants in the genus Cannabis, which includes various species or sub-species. Cannabis species in the genus include C.sativa, C.indica and C.ruderalis....
21 Jun Guidelines for Post Marketing Surveillance of Medicines and Health Products
Posted at 22:51h
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To develop a medicine information data bank on the quality of medicines in circulation and disseminate such information to stakeholders involved in the medicines supply chain. To promote communication and cooperation between stakeholders and partners involved in the medicines supply chain. To identify possible causes of inferior...
21 Jun Guideline for Release of Import Health Products at Ports of Entry
Posted at 22:47h
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This document has been prepared to serve as a guidance document regarding SAHPRA requirements for release of import health products at Ports of Entry - Regulatory Compliance Unit....
21 Jun Guidelines for Advertisement of Medicines and Health Products
Posted at 22:25h
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This document has been prepared to serve as a guidance document regarding SAHPRA requirements for advertisement of medicines and health products- Regulatory Compliance Unit....
21 Jun Guideline to Fee Determination and Payments of Permits and Related Authorisations
Posted at 22:19h
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This guideline intends to assist applicants in differentiating between various types of permits, the requirements
for each permit and the relevant fees applicable.
This guideline is applicable to Section 22A permits and related authorizations in Regulatory Compliance. The
scope includes the application process, fee applicable and...