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Essentials of Complaint Handling and Medical Device Reporting

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Website https://goo.gl/N1irBj | Edit Freely

Category fda approval for medical devices, medical device risk management, medical device recalls, fda medical device regulations, medical device training, fda regulations for medical devices

Deadline: April 20, 2017 | Date: April 20, 2017

Venue/Country: New Hyde Park, U.S.A

Updated: 2017-03-06 19:32:05 (GMT+9)

Call For Papers - CFP

Overview:

Complaint management and Medical Device Reporting (MDR) are critical quality systems for you to meet the needs of your 3 key stakeholders – the customer, the regulators, and your business. This medical device training will help you to understand the expectations of complaint handling and medical device reporting. You’ll learn about FDA expectations and regulations as well as lessons learned from 483s and warning letters. We’ll discuss how you can develop your processes to efficiently and effectively manage complaints and MDRs. In addition, we’ll discuss how to link these processes to failure investigation, recalls, and CAPA (Corrective and Preventive Action). We’ll cover best practices so you can be prepared for an FDA inspection.

Why Should You Attend:

Complaint Handling and Medical Device Reporting are considered critical processes by the FDA in maintaining the public safety. Because they are so critical they are frequently inspected areas by the FDA. More importantly, complaints can also be an early warning of issues with your products and customer problems.

Areas Covered in this Webinar:

Overview and Definitions

FDA Expectations, Regulations

Lessons Learned and Enforcement Case Studies

Processes and Procedures

Reportability Criteria

Investigating a complaint or MDR

Linkages between Complaint Handling, MDRs, and CAPA

Common Mistakes and how to avoid them

Best Practices

Preparing for an FDA or NB Inspection

Learning Objectives:

The objective of this webinar is to have an efficient and effective process for managing, analyzing, trending, and reporting product problems. This session will also cover the basics of complaint management, regulatory requirements for medical devices and medical device reporting.

Who Will Benefit:

Complaint Specialists and Managers

Individuals participating in Failure Investigations

Individuals analyzing returned products / Complaint Analysis

Regulatory Affairs

Quality Engineers

Clinical Affairs

Complaint Handling Unit Personnel

Compliance Specialists

Speaker Profile:

Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.

Susanne has a BS in Biomedical Engineering and an MBA from the University of NM. She earned her Black Belt and Master Black Belt certifications while at Johnson and Johnson. Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality.


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.