Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance

This medical device webinar will discuss strategies for meeting the Post Market Surveillance requirements as described in Annex X of the MDD (MDD 93/42/EEC, updated per the 2007/47/EEC M5 amendment, Annex 1: Essential Requirements), MEDDEV 2.7.1, Dec 2009 and ISO 14155.

Why Should You Attend:

Post Market Surveillance is a critical area in marketing medical devices and has gained tighter scrutiny by regulatory agencies over the past several years. Having appropriate and effective post market surveillance processes in place can help one avoid costly and embarrassing product recalls by being proactive rather than reactive.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

Medical device QA managers

Regulatory affairs professionals

Clinical managers or project managers

Medical device product development managers or project managers

Documentation

Instructor Profile:

Cheryl Wagoner, has 20 years of experience in quality assurance, and regulatory affairs. She currently is the Principal Consultant/Owner of Wagoner Consulting LLC, where she provides consulting services to medical device and pharmaceutical companies. Previously, she has held various positions in Quality, Regulatory, Clinical and Compliance in the medical device and pharmaceutical industries.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/clinical-evaluation-reports-medical-device-post-market-surveillance-webinar-training-703223-prdw?channel=sciencedz