Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products 2016

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

Who should Attend

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