Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel

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Category Health Care, Medical Device, Compliance Training

Deadline: April 07, 2011 | Date: April 07, 2011

Venue/Country: Wilmington, U.S.A

Updated: 2011-03-28 16:37:10 (GMT+9)

Call For Papers - CFP

Medical device firms certified to ISO 13485:2003 will find themselves very closely compliant with FDA's Quality System Requirements under 21CFR 820. This presentation will help you to understand ISO 13485 and implement a successful quality management system, comparing it to ISO 9001 and FDA & European Union requirements.

Why should you attend: International interest in certified quality systems is increasing. A Many foreign countries are now requesting medical device firm's supply them proof of certification to ISO 13485:2003. To apply a CE mark under the Medical Device Directive, 93/42/EEC, certification to ISO 13485 is required in most cases. This presentation is an in-depth analysis of ISO 13485 with comparisons to ISAO 9001.

Areas Covered in the Session:

* Principles of ISO 13485:2003

* ISO 9001 & ISO 13485 Differences

* Risk Management & ISO 14971

* FDA's MDR's & EU Vigilance

* Design Control

* MDD 93/42/EEC & Essential Requirements

Who Will Benefit:

* Manufacturing & Design Engineers

* Marketing Product Managers

* Quality System Auditors

* Quality & Regulatory Professionals

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00