Efficient and Effective FDA and ISO Management Reviews

Duration: 60 Minutes
The Webinar will discuss how to make your Management review fit your company and the best ways to get involvement from your senior management. This presentation will cover the requirement for management review from FDA cGMP and ISO 13485 and approaches that can make these effective. Management review should be a key part of keeping your quality management system efficient and effective. It will cover how to get the attention of your senior management as well as practical advice on efficient methods for conducting and documenting management reviews.
ISO 13485 training
Instructor: Betty Lane
Product ID: 500565

Why Should you Attend:
Are your management reviews effective or do you have trouble getting senior management engaged? Perhaps you are not using an effective approach that fits your company or your management. It is not only important to know what must be covered, but how to present this information to your management team. Learn how to get management's attention to the information being presented and how to make it fit your company culture. Obtain practical information on conducting and documenting management reviews.

Objectives of the Presentation:
The objectives of the presentation are to make the attendees:
  • Understand the requirements of Management Review
  • How to get Senior Management Buy-In
  • Making Management Reviews effective
  • Making Management Review fit your company culture
  • Place in Risk management
  • Conduct a Management Review
    • Agenda (Input)
    • Notice
    • Minutes (output)
Who can Benefit:
  • Quality professional with 3-15 years' experience
  • Quality professionals with the responsibility for planning or conducting management reviews
  • Quality Managers who need to make sure their company's management reviews are effective
  • Quality auditors who need to keep up to date with what ISO 13485 Auditors are expecting for Root Cause Analysis
  • Internal auditors who need to make sure their company's management reviews are effective
  • Quality engineers and others preparing information for management reviews
$375
Recorded Session for one participant
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  $500.00 Training CD
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Minimum 10 attendees
How it works
Live Session - How it works
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  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Betty Lane has over 30 years’ experience in Medical Device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems. Her work enables companies to manage their business in compliance with FDA and ISO 13485 requirements, as well quality system requirements for other area such as Europe and Canada. Her background in digital systems engineering enables her to facilitate design controls and software validation. Her areas of expertise include training, auditing, supplier management, document and records management, design controls, and software validation.

Betty’s training experience includes over 25 years of training on all areas ISO 13485 and FDA cGMP, in companies, and for AAMI, ASQ biomedical division, and ASQ sections. She has taught courses in medical quality and regulatory affairs at Northeastern University, Boston, MA. Betty is active in her local section of the American Society for Quality and is also a member of the Association for the Advancement of Medical Instrumentation (AAMI), The Society of Women Engineers and the IEEE. Betty has degrees in engineering from Rensselaer Polytechnic Institute (RPI), and an MBA from Northeastern University.
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