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.

Online PR News – 19-June-2012 – Palo Alto – Palo Alto, CA, USA – June 16, 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 and participants will be eligible to receive up to 12 RAC credits toward their certification.

For more information or to register for the seminar, please click here.

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. He is a regular speaker at international conferences including ASQ, ISM, and RAMS.

In this interactive seminar, Mr. O’Leary will teach participants how to classify devices, select the appropriate conformity assessment path, prepare the required documentation, and maintain it. The course will also include exercises that apply the principles and help solidify learning.

Mr. O’Leary will address the details of the MDD and includes other significant issues such as the Quality Management System (ISO 13485), Risk Management (ISO 14971), Clinical Evaluation (MDD Annex X), and the role of harmonized standards.

Participants will learn how to integrate the Clinical Requirements in the MDD into the essential requirements and risk management processes.

This course will benefit anyone involved in quality or regulatory compliance for medical devices marketed in the European Union and is ideal for quality, regulatory, and clinical professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors. Regulatory managers, quality managers and directors, marketing managers, clinical managers and export compliance managers will find this course useful.

Date: Thursday, July 19 & Friday, July 20, 2012, 9 AM to 5 PM EDT

Venue: Hampton Inn Philadelphia City Center, PA

Registration Cost: $999 per registration

Early bird discounts: For discounts on early registrations, please click here.

Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to

For more information on ComplianceOnline or to browse through our trainings, please visit our website.

About ComplianceOnline
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,000 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at
For more information please contact:

A Reuben Bernard
Manager of Program Marketing
2600 E Bayshore Rd
Palo Alto CA USA 94303
650-620-3937 phone
650-963-2530 fax

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