Learning Design Controls through Review of FDA 483 Observations 2016

Learning Design Controls through Review of FDA 483 Observations 2016 is a webinar dedicated to medical device design controls.

Learning Design Controls through Review of FDA 483 Observations 2016 is a webinar that covers topics such as:

• Design Inputs
• Design and Development Planning
• Design Reviews
• Design Output
• Design Validation
• Design Verification
• Risk Management
• Design Transfer

Learning Design Controls through Review of FDA 483 Observations 2016 is intended for attendees from medical device companies:

• Developers
• Quality Assurance Engineers
• Quality Auditors
• Systems Engineers
• Documentation specialists
• Engineering Managers
• Manufacturing Engineers