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Industry Workshop on FAQs and Common Deficiencies for APIMF Submission
June 28 @ 9:00 am - 10:30 am
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 APIMF submission procedure. In addition, it highlighted the information on the FAQ/common deficiencies evaluators encounter when assessing the API.
Download Presentations
- APIMF Submissions
- FAQs & Common Deficiencies for APIMF Submission Documents
- GMP Requirements for APIs
Watch Recording