FDA Compliance and GAMP V Computer System Classification 2016 is a webinar that covers topics such as:
- Develop the ability to apply GAMP V in classifying computer systems in your organization
- GAMP V computer system classifications
- Best practices necessary to ensure all systems are classified properly and validated appropriately
- The level of computer system validation required, based on the classification as determined using GAMP V
- 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
- 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
- The level of training required for the various GAMP V computer system classifications, and the skills and expertise necessary to make the classification determination
- How to gain information about trends in validation, as industry progresses and new best practices emerge
FDA Compliance and GAMP V Computer System Classification 2016 is intended for senior attendees involved or interested in:
- QC/QA Managers and Analysts
- Information Technology Analysts
- Analytical Chemists
- Clinical Data Managers and Scientists
- Lab Managers
- Compliance Managers
- Computer System Validation Specialists
- Automation Analysts
- Business stakeholders and individuals who are responsible for CSV planning, execution, reporting, compliance, and audit
- GMP Training Specialists
- Consultants