The FDA Issues Draft Guidance for 3D Printed Medical Devices 2016 is a webinar that covers topics such as:
- 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
The FDA Issues Draft Guidance for 3D Printed Medical Devices 2016 is intended for:
- 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
