Here is the updated list of few upcoming webinar on medical device -
1. The EU Clinical Trial Directive
2. Preparing and Executing Medical Device Quality Audits: How to Meet the FDA’s Expectations
3. Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137
4. Risk Management - Do Not Throw Dice on Your Company!
5. Maintaining a Sustainable and Compliant Design Validation System and Using FMEA for Device Manufacturers
6. Risk and Hazard Assessment for Medical Devices - ISO 14971
7. New Medical Device Vigilance Guidelines
Source: ComplianceOnline
Thursday, April 09, 2009
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