This webinar will discuss current regulatory and quality requirements for reduced testing of components used in pharmaceuticals and medical devices. Reduced testing will be viewed from current industry practice, the regulations, and quality principles. The reduced testing lifecycle we studied and reviewed. This includes such topics as component specifications, material qualification, supplier auditing and qualification, collaborative laboratory testing, certificates of analysis, material validation sampling, analyzing testing, qualification, and disqualification. Examples of systems will be shown. This webinar will primarily use graphics, especially flowcharts, to demonstrate the principles and increase in understanding of the topics.
Applying GMP Quality Principles To Establish A Reduced Testing Program
18 August 2011, Houston, United States
Introduction
Venue
Online Webinar
Online Webinar, 10777 Westheimer Suite 1100, Houston, United States
Organised by
Compliance2GO
Contact information
Compliance2GO Customer Support
10777 Westheimer Suite 1100, Houston, United States of America
877-782-4696
Contact us by email
10777 Westheimer Suite 1100, Houston, United States of America
877-782-4696
Contact us by email
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