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Fast Facts

Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel

Jun 06,2012 - Jun 06,2012
Online Training, Wilmington, Delaware, United States
 

Highlights

Overview: The FDA's Quality System Regulation (QSR) prescribes the Quality Management System for a medical device manufacturer who markets in the US. 

ISO 13485 covers the rest of the world. The webinar describes management responsibility by reviewing the regulations and the reasoning that FDA published. Management responsibility, in QSR, has five major components: Quality Policy, Organization, Management Review, Quality Planning, and Quality System Procedures. The webinar covers each of these topics and provides a list of things you should consider in your implementation.

Why should you attend: One of the most common areas for FDA Warning Letters is Management Responsibility. FDA considers this a principle subsystem and is where they start inspections. Ensuring that you understand what they expect and how to implement it is a valuable approach to preventing problems. More than that, however, a company can achieve tremendous value by setting up the FDA system. Effective management reviews, for example, can help your company identify opportunities for improvement, resolve issues, and make better products at lower cost. Quality plans and document structure outlines can help ensure you have covered all the requirements, i.e., no gaps, but that you haven’t duplicated effort or created redundant procedures.

Areas Covered in the Session:

  • Valuable documents that provide understanding
    • Quality System Regulation (QSR), including the definitions
    • QSR Preamble
    • ISO 13485:2003
    • FDA's Quality System Inspection Technique (QSIT) manual
    • Warning Letters
  • Subject Areas covered
    • Quality policy
    • Organization
    • Responsibility and authority
    • Resources
    • Management Representative
    • Management review
    • Quality planning
    • Quality system procedures
  • For each subject area, the webinar includes information from the valuable documents listed above
Who will benefit:
  • Device Company Executives
  • Device company Managers
  • Quality Managers
  • Regulatory Affairs Managers
  • Risk Managers
  • Management Representatives
  • Production Managers
  • Design Engineering Managers

Price List:Live : $245.00Corporate live : $995.00Recorded : $295.00
webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com
Phone: 800-447-9407Fax: 302-288-6884











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Event Profile

Sponsors: GlobalCompliancePanel
Speakers: Dan OLeary
Attendees: Device Company Executives,Device company Managers,Quality Managers,Regulatory Affairs Managers

Contact Details

Contact person: webinars
Event website: http://bit.ly/HrTt9Z
Phone: 800-447-9407
Fax: 302-288-6884

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