Pharma Licencing Guidelines

Document Number	Title	Categories	Date Updated	Version	Units	File Type	Link	doc_categories_hfilter	doc_tags_hfilter
SAHPGL-INSP-06	Guideline for Fee determination and Payment of GxP and Product related Inspection	Guideline	14/09/2022	2	Inspectorate and good manufacturing practices	pdf	Download	guideline	inspectorate-and-good-manufacturing-practices
SAHPGL-INSP-05	Guideline on how to respond to a GMP, GWP, GCP and GVP Inspection report	Guideline	21/09/2022	2	Inspectorate and good manufacturing practices	pdf	Download	guideline	inspectorate-and-good-manufacturing-practices
SAHPGL-INSP-04	Guideline for preparation of site master file	Guideline	14/09/2022	5	Inspectorate and good manufacturing practices, Licencing	pdf	Download	guideline	inspectorate-and-good-manufacturing-practices licencing
SAHPGL-INSP-03	Guideline for Good Wholesaling Practice for Wholesaler	Guideline	07/09/2022	5	Inspectorate and good manufacturing practices, Licencing	pdf	Download	guideline	inspectorate-and-good-manufacturing-practices licencing
SAHPGL-INSP-01	Guideline for Post Importation Testing	Guideline	15/09/2022	5	Inspectorate and good manufacturing practices	pdf	Download	guideline	inspectorate-and-good-manufacturing-practices
SAHPGL-INSP-02	Guideline for Good Manufacturing Practice	Guideline	18/09/2022	8	General ECTD & human medicines, Inspectorate and good manufacturing practices, Licencing	pdf	Download	guideline	general-ectd-human-medicines-guidelines inspectorate-and-good-manufacturing-practices licencing