FDA Issues Draft Guidance for 3D Printed Medical Devices 2016
20 Jul 2016
Webinar
Description
Topics
FDA Guidance
Applicable Laws and Regulations
Considerations for 3D Design and Manufacturing
Definitions
Considerations for Quality Data
Requirements for Process Validation
Labeling
Device Testing Requirements
3D Examples of Medical Devices
Who should Attend
Compliance Officers
Healthcare industry: drugs, biologics, medical devices/IVDs, combination products, etc
Clinical Affairs
Regulatory Affairs
Laboratory Personnel
Quality Assurance
Consultants
R&D Professionals
Contractors/Subcontractors
Other professionals interested in this topic
Past Events
FDA Issues Draft Guidance for 3D Printed Medical Devices 2016 - 20 Jul 2016, Webinar (60563)
Important
Please, check "FDA Issues Draft Guidance for 3D Printed Medical Devices" official website for possible changes, before making any traveling arrangements
