POLICY ON MANAGEMENT OF POTENTIAL …

MEDICINES CONTROL COUNCIL POLICY ON MANAGEMENT OF POTENTIAL CONFLICT OF INTEREST NOVEMBER 2011. 1 INTRODUCTION. Section 6(4) of the Medicines and Related Substances Act 101 of 1965 “The ,

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SOUTH AFRICAN HEALTH PRODUCTS …

www.ursonline.co.za URS 24099 The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act,

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Registration of Medicines Stability MEDICINES …

Registration of Medicines Stability 2.05_Stability_Jul12_v7_1 Page August 2012 1 of 27 MEDICINES CONTROL COUNCIL STABILITY This guideline is intended to provide recommendations to applicants wishing to submit applications for the registration of

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MEDICINES CONTROL COUNCIL - sahpra.org.za

Registration of Medicines CMs DS Safety & Efficacy 7.01_CMs_SE_DS_Jun16_v3.doc June 2016 Page 1 of 46 MEDICINES CONTROL COUNCIL COMPLEMENTARY MEDICINES - DISCIPLINE-SPECIFIC

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MEDICINES CONTROL COUNCIL - sahpra.org.za

Registration of Medicines Amendments . 2.08_Amendments_Jul12_v6_showing_changes August 2012 . Page 1 of 43. MEDICINES CONTROL COUNCIL . AMENDMENTS

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Medicines Control Council - sahpra.org.za

Registration of Medicines Reporting of Adverse Drug Reactions 2.11_ADR_reporting_May03_v1_2.doc December 2012 Page 2 of 18 TABLE OF CONTENTS Page 1 Introduction 4

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MEDICINES CONTROL COUNCIL - sahpra.org.za

Annex 12 Use of ionising radiation in the manufacture of medicinal products – cont. 12.5.1 . General : 96 . 12.5.2 : Gamma irradiators A Design . 96

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MEDICINES CONTROL COUNCIL - sahpra.org.za

6.01 MRF1 Medicine Registration Application (Human) - replaced by ZA-CTD . 6.02 MRF2 Screening of Application* 6.03 MRF4 Package Insert Amendments*

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MEDICINES CONTROL COUNCIL - sahpra.org.za

This document is intendedto serve as guidance on the requirements for Good Manufacturing Practice in South Africa. This guideline is not intended as an exclusive approach.

Government Gazette Staatskoerant - sahpra.org.za

"(z) the category of medicine immediately preceding the registration or application number; (aa) the pharmacological classification of the medicine; and

MEDICINES AND RELATED SUBSTANCES CONTROL ACT …

1 MEDICINES AND RELATED SUBSTANCES ACT, 1965 (ACT 101 OF 1965) NOTE: The whole of this Act, except sections 1, 15B, 18, 22B, 24, 34A and 40, has been repealed by section 50 of the South African Medicines and Medical Devices …

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Medicines Control Council : General Information

Substances Act, 1965 (Act 101 of 1965), and the Regulations to this Act. 1 INTRODUCTION The registration of medicine in South Africa is governed by the provisions and requirements of the Medicines and Related Substances Control Act No. 101 of 1965, (hereafter 'the Act') and the Regulations and Guidelines published in terms thereof.

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Policy and Procedures for the disposal of pharmaceutical waste

medicines and Related Substances Act (Act 101 of 1965) as amended. Additional minimum standards to Annexure A of the Rules relating to good pharmacy practice in terms of section 35A(b)(ii) of the Pharmacy Act 53 of 1974, as amended, were published in Board Notice 34 of 2012, regarding destruction and disposal of medicines and scheduled substances.

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OCCUPATIONAL SAFETY

Workplace Component of Republic Act No. 8504 otherwise known as the “Philippines AIDS Prevention and Control Act of 1998” and its Implementing Rules and Regulations Department Order No. 16-01 - Series of 2001- Rule 1030 Training and Accreditation 262 of Personnel on Occupational Safety and Health

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Medical Office Policy and Procedure Manual

Medical Office Policy and Procedure Manual Company Name, Inc. 1234 Second Ave. San Diego, CA 92101, USA Tel: +1. 858.321.1234 Fax: +1. 858.321.5678

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