System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2015
12 Aug 2015
Webinar
Key Topics
How to develop the ability to apply the SDLC when validating computer systems in your organization
System Development Life Cycle (SDLC) Methodology
How to ensure all systems are validated appropriately
R maintaining a computer system in a validated state
How to effectively document the process of computer system validation, and maintain current information about the various systems in your organization and how they are maintained in a validated state
How to develop the appropriate computer validation strategy, to ensure a good balance of cost vs. risk
Some of the key "pitfalls" to avoid when applying the SDLC methodology
How to gain information about trends in validation, as industry progresses and new best practices emerge
Who should Attend
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
Maintenance and audit. This webinar will also benefit any consultants working in the life sciences industry who are involved in computer system implementation
Compliance
Validation and compliance
Past Events
System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2015 - 12 Aug 2015, Webinar (53462)
System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2026
Important
Please, check "System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems" official website for possible changes, before making any traveling arrangements
