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PHARMACOVIGILANCE GUIDELINES

Document NumberTitleCategoriesDate UpdatedVersionUnitsFile TypeLinkdoc_categories_hfilterdoc_tags_hfilter
PV-FRW-03National Vigilance Framework28/10/20251pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-03Risk Management Plans for Medicines for Human Use15/09/20221pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-04Post-marketing Reporting of Adverse Drug Reactions for Human Medicines in South Africa22/09/202510pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-02Pharmacovigilance systems06/06/20232pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-01Pharmacovigilance Inspections for Human Medicinal Products10/05/20221pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-05Guideline for the handling of Dear Healthcare Professional Letters relating to medicine safety25/08/20226pdfDownloadguidelinepharmacovigilance
SAHPGL-CEM-PV-06Guideline for Adverse Drug Reactions (ADRs) Reporting for Healthcare Professionals23/10/20254pdfDownloadguidelinepharmacovigilance