This session will discuss key considerations for Good Documentation Practices that would impact product quality, safety, and efficacy and/or data integrity. Key components of documentation and record management system will be introduced. Regulatory requirements will also be discussed as the basis of documentation standards. It will also cover different types of records and how it would affect quality systems.
2-day In-person Seminar on The A to Z's of Writing and Enforcing Effective SOPs (Standard Operating Procedures) at Atlantic city, NJ
13 - 14 April 2014, Atlantic city, NJ, United States
Introduction
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WILL BE ANNOUNCED SOON
WILL BE ANNOUNCED SOON, Atlantic city, NJ, Atlantic city, NJ, United States
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GlobalCompliancePanel
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