Learning Design Controls through Review of FDA 483 Observations 2016
12 Oct 2016
Webinar
Learning Design Controls through Review of FDA 483 Observations 2016 is a webinar dedicated to medical device design controls.
Key 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
Past Events
Learning Design Controls through Review of FDA 483 Observations 2016 - 12 Oct 2016, Webinar (62754)
Learning Design Controls through Review of FDA 483 Observations 2026
Important
Please, check "Learning Design Controls through Review of FDA 483 Observations" official website for possible changes, before making any traveling arrangements
