Learning Design Controls through Review of FDA 483 Observations 2016 is a webinar dedicated to medical device design controls.
Topics
- Design Inputs
- Design and Development Planning
- Design Reviews
- Design Output
- Design Validation
- Design Verification
- Risk Management
- Design Transfer
Who should Attend
Attendees from medical device companies:
- Developers
- Quality Assurance Engineers
- Quality Auditors
- Systems Engineers
- Documentation specialists
- Engineering Managers
- Manufacturing Engineers
