System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2015 is a webinar that covers topics such as:
- 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
System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2015 is intended for:
- 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