Ensuring Your Site is Ready for an FDA Inspection

Date : 22nd January 2020 to 22nd January 2020

Place : United States, Aurora

Website :http://bit.ly/2SRgvRU

Contact Person:Training Doyens

Description:

Learn how to manage an FDA inspection and avoid 483s and warning letters. The webinar discusses FDA audit preparation checklist, quality management system, subject matter expert training and more.

Ensuring Your Site is Ready for an FDA Inspection will be held in Aurora,United States on date 2020-01-22

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Deadline for abstracts/proposals : 22nd January 2020

Keynote Speakers : Susanne Manz 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. She 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.

Conference Highlights :OVERVIEW Although an effective Quality Management System should always be inspection ready, many medical device companies make basic mistakes during FDA inspections leading to 483s and even warning letters. This webinar will help you create an inspection readiness plan, so you are well prepared for an FDA inspection. WHY SHOULD YOU ATTEND An FDA inspection can be a very stressful and challenging experience. These stresses can lead even experienced people to make very costly mistakes during a

Venue :Training Doyens, East Walker Drive, Aurora, CO, USA

Check the event website for more details.