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Pharmaceutical Tag

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19 Jun

Posted at 14:45h in

The South African Health Products Regulatory Authority (SAHPRA) hosted an industry workshop to empower and educate you on the FAQs & Common Deficiencies for APIMF [Active Pharmaceutical Ingredient Master File] Submission. The workshop provided information to the Industry Stakeholders and APIMF holders on the SAHPRA’s current...

04 Apr

Posted at 20:30h in

The South African Health Products Regulatory Authority (SAHPRA) hosted an industry workshop to empower and educate you on the Authority’s requirements when submitting Risk Management Plans (RMPs). This workshop highlighted the importance of maintaining RMPs to ensure the safety of medicines, while also sharing requirements for compliance. Date: 11 April...