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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

There may be many networking opportunities at the Post-Market Compliance for Medical Devices and Evolving Reporting Requirements: Complaint Handling, MDR/eMDR and Recalls including UDI update. Find out more in the event details below.

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Website: http://www.complianceonline.com/complaint-handling-medical-device-repo...
Conference/Event Dates: 08/06/2015 - 08/07/2015
Conference/Event Hours: 08:30 AM to 12:00 PM
Classification: B2B
Primary Industry: Sciences
Other Industries: Business, Sciences
Estimated Attendance: 30
Cost to Attend: One Registration: $1499
Audience: Regulatory Affairs
QA/QC
Project Managers
Regulatory Professional
Risk Managers
Venue: Courtyard Minneapolis Downtown
Venue Phone: (612) 333-4646
Venue Type: Indoor - Hotel
Show Owner:ComplianceOnline

Booth Size Booth Cost   Available Amenities
Call for information.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: Call
Other Booth Sizes Available: n/a

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Post-Market Compliance for Medical Devices and Evolving Reporting Requirements: Complaint Handling, MDR/eMDR and Recalls including UDI update

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