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EVENT DATES
Aug 2015
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Venue

Courtyard Minneapolis Downtown 1500 Washington Ave South Minneapolis , Minnesota 55454
Tel: (612) 333-4646
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Post-Market Compliance for Medical Devices and Evolving Reporting Requirements: Complaint Handling, MDR/eMDR and Recalls including UDI update

30 0

Overview

This interactive one and a half day course led by Ms. Rita Hoffman, Former FDA CDRH Recall Branch Chief, who has more than 36 years’ experience with the FDA will provide the participants tools to minimize risk of regulatory enforcement actions.

Learning Objectives:
Understand how to comply with complicated Compliant Handling, MDR and Recall requirements.
Firms MDR reporting and FDA's handling of reports.
Company preparation in the event of a Recall, recall strategy, notification letter and communicating with the FDA.
Minimize your risk of regulatory enforcement actions.

Who will Benefit:
This course will benefit anyone in the medical device industry that handles functions involving product complaints, recalls, medical device reporting.

Regulatory Affairs
QA/QC
Project Managers
Regulatory Professional
Risk Managers

Note:
Use coupon code 232082 and get 10% off on registration.

For Registration:
http://www.complianceonline.com/complaint-handling-medical-device-reporting-and-recalls-seminar-training-80068SEM-prdsm?channel=eventsinamerica

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