You should attend this seminar if you are responsible for planning, executing or managing the implementation of any system governed by FDA regulations, or if you are maintaining or supporting such a system.
We will discuss the importance of classifying computer systems subject to FDA regulations in accordance with GAMP5. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do.
Areas to be Covered:
Gain an understanding of GAMP V computer system classifications
Develop the ability to apply GAMP V in classifying computer systems in your organization
Understand the level of computer system validation required, based on the classification as determined using GAMP V
Discuss the best practices necessary to ensure all systems are classified properly and validated appropriately
Learn how to develop the appropriate computer validation strategy, including the level of testing required for the given computer system classification, as determined by GAMP V
Understand how to effectively document the process of computer system classification and how to maintain current information about the various systems in your organization and how they are validated
Learn how to gain information about trends in validation, as industry progresses and new best practices emerge
Understand the level of training required for the various GAMP V computer system classifications, and the skills and expertise necessary to make the classification determination
Industry Best Practices
Who will Benefit:
This webinar is intended for those working in the FDA-regulated industries, including pharmaceutical, medical device, biological, animal health and tobacco. Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, adverse events management and post-marketing surveillance.
Information Technology Analysts
Information Technology Developers and Testers
QC/QA Managers and Analysts
Clinical Data Managers and Scientists
Compliance and Audit Managers
Computer System Validation Specialists
GMP Training Specialists
Business Stakeholders/Subject Matter Experts
Business System/Application Testers