Clinical Evaluation and Risk Management

This webinar explains each system, and show how they are related. The webinar uses guidance documents from the EU and the GHTF to help explain the systems and clarify the regulatory expectations.
When the European Union's changes to the Medical Device Directive (MDD) went into effect in March 2010, it created a requirement for Clinical Evaluation.

GlobalCompliancePanel

Phone: 800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com