System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems 2015

  • 12 Aug 2015
  • Webinar

Description

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

Past Events

Important

Please, check "System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations

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