ComplianceOnline

Integrating Risk Management with the Quality System

Instructor: Edwin L Bills
Product ID: 701447
Training Level: Advanced
  • Duration: 85 Min

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Oct-2009

Training CD / USB Drive

$500.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This Risk Management training will discuss how to develop a compliant risk management process as a part of medical device Quality System built as per ISO 14971 standards.

Why should you Attend:
As the European Union Medical Device Directive changes are moving forward, more Notified Bodies are upgrading their approach to medical device risk management. The FDA is now citing manufacturers for risk management issues and these are starting to appear in Warning Letters. With the renewed emphasis on Enforcement by FDA, and more scrutiny in the premarket application arena, manufacturers need to upgrade their approach to Risk Management to fully comply with the ISO 14971 Risk Management standard. ISO 14971 is the FDA recognized standard and is also the Harmonized Standard in the EU scheme for medical devices.

Companies are continuing to upgrade their Quality Systems to include new concepts of Risk Management. This presentation has been updated to include some example forms and flow charts for an integrated risk management and quality system. This presentation will provide guidance on developing a fully compliant Risk Management process as part of the medical device Quality System. Manufacturers can use this presentation to guide their improvements in developing a compliant risk management process fully integrated into the quality system.

Areas Covered in the seminar:

  • How to use the Risk Traceability Summary to document Risk Management activities during design, production and post-production.
  • Examining Risk Management requirements for each phase of the product lifecycle.
  • Identifying documentation requirements for Risk Management.
  • Developing forms and reports that provide objective evidence of risk management compliance.
  • Integrating Postmarket Risk Management activities with CAPA.
  • How FDA's Health Hazard Evaluation relates to Risk Management.
  • How Risk Management Tools relate to documentation of Risk Management activities.

Who will benefit:

  • Regulatory Affairs personnel
  • Regulatory Affairs Managers
  • Qualtiy Managers
  • Quality Assurance Engineers
  • Design Managers
  • Process Engineering
  • Risk Managers

Instructor Profile:
Edwin L. Bills, is the Principal Consultant for Bilanx Consulting LLC, a consulting firm that provides assistance to medical device companies in compliance with US FDA regulations, in development of Quality Management Systems and Risk Management processes. Edwin has over 20 years experience in the medical device industry and has participated in development of industry standards, including ISO 14971. In his consulting role he has assisted companies in Warning Letter responses. Edwin has also participated in training both company and FDA personnel in the Quality System Regulation and Product Risk Management.

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Upcoming In-person Seminars by EX-FDA OFFICIALS
Risk Management in Medical Devices Industry

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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