Here is the updated list of few upcoming webinar on medical device –
- The EU Clinical Trial Directive
- Preparing and Executing Medical Device Quality Audits: How to Meet the FDA’s Expectations
- Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137
- Risk Management – Do Not Throw Dice on Your Company!
- Maintaining a Sustainable and Compliant Design Validation System and Using FMEA for Device Manufacturers
- Risk and Hazard Assessment for Medical Devices – ISO 14971
- New Medical Device Vigilance Guidelines