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Doc#	Title	Version	SubVersion	PublishDate	Size
16.04	Licence to act as a Wholesaler of Medical Devices & IVDs	V1		03-Aug-2017	103 KB
2.04	Post-importation Testing	V2		20-Jan-2017	526 KB
2.04	Post-importation testing showing changes	V2		20-Jan-2017	509 KB
2.11	Safety Reporting during Clinical Trials in South Africa	V2		20-Aug-2016	424 KB
2.40	Clinical Trial Oversight, Monitoring of Clinical Trials	V1		10-May-2016	162 KB
2.42	Post Clinical Trial Drug Access	V1		10-May-2016	98 KB
2.45	Borderline Products	V1		30-Mar-2017	795 KB
2.46	Co-packaging of Medicines	V1		05-May-2017	93 KB
2.48	Exemptions from certain medicine registration requirements for Human Medicines – for comment	V1		30-Dec-2017	99 KB
2.49	Capacity Building and Transformation in Clinical Trials Research in South Africa	V1		10-Mar-2018	99 KB
2.50	Medicines and Human Reproduction for comment	V1		02-May-2018	286 KB
5.07	Guideline for recall / withdrawal of Medicines, Medical devices and IVDs – for comment	V4		21-Sep-2015	314 KB
5.07	Guideline for recall / withdrawal of Medicines, Medical devices and IVDs – showing changes	V4		21-Sep-2015	316 KB
6.1.a	Biological Amendments	V1		19-Jun-2017	1 MB
7.04	Complementary Medicines – Health Supplements Safety & Efficacy	V3		12-Apr-2017	680 KB
7.04	Complementary Medicines Health Supplements Safety & Efficacy Annexure J	V3	3.1	30-May-2017	408 KB
7.06	Complementary Medicines – Caffeine and Menthol	V1		12-Apr-2017	100 KB
8.01	General Information – Medical Devices and IVDs for comment	V2		23-Sep-2015	807 KB
8.03	Conformity Assessment Procedures – Medical Devices and IVDs for comment	V1		23-Sep-2015	407 KB
8.04	ADR and Post-Marketing Vigilance Reporting of Medical Devices and IVDs for comment	V1		23-Sep-2015	165 KB

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