ComplianceOnline Announces Seminar on Understanding and Implementing EU Medical Device Directive
ComplianceOnline, the leading GRC advisory network, and medical device quality expert Dan O'Leary, will conduct a two-day long, in-person seminar on understanding and implementing the EU Medical Device Directive.
- Philadelphia, PA-NJ (1888PressRelease) June 19, 2012 - ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on Understanding and Implementing the Medical Device Directive. The two day long, in-person seminar, led by medical device quality expert Dan O'Leary, will be held on July 19 and 20, 2012 in Philadelphia, PA.
The seminar will help attendees comprehensively understand details of the EU MDD and implement its requirements. The course has been pre-approved by RAPS.
Seminar instructor Dan O'Leary has more than 30 years of experience in quality, operations and program management in regulated industries including aviation, defense, medical devices, and clinical labs.
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