10 Apr Communication Regarding the Development of a Policy Relating to the Issuing of Licences in Terms of Section 22c(1)(B) of the Medicines and Related Substances Act, 101 of 1965, in Accordance With Broad-based Black Economic Empowerment Principles
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The South African Health Products Regulatory Authority (SAHPRA) is a statutory body established in terms of Section 2 of the Medicines and Related Substances Act, 101 of 1965, as amended. The objects of the Authority are to provide for the monitoring, evaluation, regulation, investigation, inspection, registration, and control of health products (medicines and medical devices), scheduled substances, clinical trials, and related matters in the public interest.
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Document Number:
Leg01-2024/25
Version:
1
Date Updated:
10/04/2025
File Type:
pdf
Category:
Communication to industry