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    Document Control Recommended Practice: A guide for implementation and audit purposes (Augmented Edition - 3rd Edition) (English Edition)

    Beschreibung Document Control Recommended Practice: A guide for implementation and audit purposes (Augmented Edition - 3rd Edition) (English Edition). Augmented Edition (3rd Edition)This short guide provides you with the list of all the essential elements that a proper Document Control system should entail (document numbering, revision system, quality control, etc). It is a practical tool that can be used as a guidance for implementing a Document Control System, or for enhancing or auditing an existing one.The requirements are intended to be applicable to all organizations, regardless of the type, the size and the nature of their activities. The Recommended Practice captures the minimum business requirements to be implemented in an efficient, quality-oriented and fit-for-purpose Document Control System.Table of Content:1. SCOPE2. IDENTIFICATION OF DOCUMENTS2.1. UNIQUE IDENTIFICATION NUMBER2.2. DOCUMENT TEMPLATE2.3. QUALITY CHECKS2.4. REGISTER OF DOCUMENTS3. DOCUMENT MODIFICATIONS3.1. REVISION SYSTEM3.2. MODIFICATIONS4. REVIEW AND APPROVAL OF DOCUMENTS5. CONTROL OF THE CONTENT5.1. RELEVANT REVISIONS5.2. DISTINCTION BETWEEN WORKING DOCUMENTS AND OFFICIAL DOCUMENTS5.3. DISTRIBUTION5.4. TRANSMITTAL5.5. TRACEABILITY6. DOCUMENTED PROCEDURE



    Buch Document Control Recommended Practice: A guide for implementation and audit purposes (Augmented Edition - 3rd Edition) (English Edition) PDF ePub

    Audit Policy Recommendations / Microsoft Docs ~ These recommendations are meant to provide a baseline guide for the administrator. All recommendations should be thoroughly reviewed prior to implementation in a production environment. Refer to Appendix L: Events to Monitor for a list of the recommended events to monitor, their criticality ratings, and an event message summary.

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    WHO good manufacturing practices for pharmaceutical ~ manufacturing practice in the manufacture and quality control of medicines and pharmaceutical specialities and was accepted. The revised text was discussed by the WHO Expert Committee on Specifications for Pharmaceutical Preparations in 1968 and published as an annex to its twenty-second report. The text was then reproduced (with some revisions) in 1971 in the Supplement to the second edition .

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