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Guide: Best Practices for Quality Agreements Version 2.0

17 April 2018
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Template / Tool

GMP Audit Manual – Data Governance and Data Integrity

27 March 2018
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Data Integrity Library

13 March 2017
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FDA Office of Generic Drugs Issues 2016 Annual Report

10 March 2017
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CDER Issues Updated CY2017 Guidance Agenda

10 March 2017
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WHO issues draft guidance: “Testing of Suspect Spurious/Falsely-Labelled/Falsified Counterfeit Medicines”

18 November 2016
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Supplier Assessment Questionnaire Kit

9 November 2016
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Document

Rx-360 Audit Guide for Basic Chemicals and Raw Materials

11 July 2016
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Rx-360 Supply Chain Security Checklist for Auditors

28 June 2016
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Survey: Upstream Supply Chain Security Working Group

14 April 2016
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