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FDA Inspection 2020 : How to Prepare for and Manage an FDA Inspection

Online
Event Date: Feb 24, 2020 - Feb 24, 2020

About

Overview

Are you ready for the FDA to knock on your door? Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This webinar can help you manage inspections efficiently and effectively. A professional, polished, responsive approach sets a good tone for an inspection. You will learn how to present information about your quality system in the most competent and professional manner.

Why should you attend this webinar?

An FDA inspection can be a very stressful and challenging experience. These stresses can lead even experienced people to make very costly mistakes during an inspection. But good preparation can ease the stresses and lead to much more favorable results. This webinar can help you prepare a strategy and detailed plans to more successfully prepare for, manage, and respond to an FDA Inspection. If you?ve had a recall, an increase in MDRs, or it?s been more than 2 years since your last inspection, you can benefit from this webinar.

Call For Paper

Areas Covered in the Session:

  • FDA Inspectional approach
  • Inspection strategy and planning
  • Preparing
  • How to manage an inspection
  • Key roles during an inspection
  • Training for SMEs (Subject Matter Experts) and other roles
  • Do's and Don'ts
  • Common mistakes to avoid
  • How to respond to inspection observations

Who can Benefit:

  • Quality Engineers
  • Compliance Specialists
  • Compliance Managers and Directors
  • Quality Managers and Directors
  • Consultants and Contractors
  • Business Leaders wishing to present a professional and compliant organization
  • Cross-functional leaders wanting to make sure their organizations are well prepared
  • Anyone involved with an FDA or NB inspection

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