Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products 2016 is a webinar focused on
- The computer system validation planning, execution and management concepts
- Most current FDA regulations for tobacco products and the systems that affect them
- Steps required for a compliant validation process, along with the key documentation associated with maintaining the systems in a validated state, while minimizing costs
- How to be adequately documented to meet FDA requirements for tobacco-related products
- How to leverage these practices across all systems by creating a standardized program for their organization
Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products 2016 is intended for attendees from:
- 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 computer system validation planning
- GMP training specialists
- Reporting
- Execution
- And audit. This webinar will also benefit any consultants working in the tobacco industry who are involved in computer system implementation
- Compliance
- Validation and compliance
