THIS WEBINAR WILL DISCUSS HOW TO IMPLEMENT MEDICAL 2013 - Medical Device Complaint Handling Systems

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THIS WEBINAR WILL DISCUSS HOW TO IMPLEMENT MEDICAL 2013 - Medical Device Complaint Handling Systems - Webinar By GlobalCompliancePanel

Website http://bit.ly/16L7Fra | Edit Freely

Category Webinar, Health, Pharma, Medical Device, FDA, Clinical

Deadline: June 11, 2013 | Date: June 11, 2013

Venue/Country: California, U.S.A

Updated: 2013-05-22 15:41:29 (GMT+9)

Call For Papers - CFP

Overview: This webinar is intended to demonstrate how to adequately establish and maintain medical device complaint handling systems. All medical device manufacturers are required to comply with the complaint handling requirements. Understanding the relevant and applicable requirement can significantly contribute to achieving compliance and remaining compliant, resulting in saving significant amount of time and efforts in business while ensuring the safety and effectiveness of the medical device products.

This webinar will discuss how to implement medical device complaint handling procedures, how to achieve compliance, and how to remain compliant. At the end of the webinar, you will get familiarized with the FDA-compliant system for handling all types of medical device complaints.

Why Should You Attend: FDA regulations require all medical device manufacturers to comply with the complaint requirements. This webinar will discuss how to adequately establish and maintain medical device complaint handling systems.

Areas Covered in the Session:

Applicable statutes and regulations for medical device complaint handling

Definitions

What to do when complaints are received?

How to process complaints.

What processes need to be in place?

When to investigate complaints.

When to open a CAPA(s).

Investigation and documentation requirements

Relationship between complaints, MDR, and CAPA

Enforcement actions: numerous case studies

Lessons learned

Who Will Benefit:

CEOs

VPs

Compliance Officers

Attorneys

Complaint Handling Personnel

Clinical Affairs

Regulatory Affairs

Quality Assurance

R&D

CROs

Consultants

Contractors/subcontractors

Dr. Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal “Science.” Since then, Dr. Lim has held various positions at Duke, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences, Inc., A Luminex Company.

NetZealous LLC,

DBA GlobalCompliancePanel

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Suite 216, Fremont, CA 94539, USA

USA Phone:800-447-9407

Fax: 302-288-6884

webinarsglobalcompliancepanel.com

http://www.globalcompliancepanel.com

Event Link - http://bit.ly/18dZ1PX

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.