How to prepare for and host an FDA inspection and respond to 483'

Date : 24th October 2018 to 24th October 2018

Place : United States, Aurora

Website :https://bit.ly/2QXpOg6

Contact Person:Training Doyens

Description:

OVERVIEW In this webinar you will learn about the types of FDA inspections, preparations such as assigning personnel to specific tasks for the FDA inspection, facility requirements to support the inspection (front room, back room), the value of mock audits, how personnel should conduct themselves during the inspection, the inspection process and techniques for responding to 483s and warning letters. How to respond and when is critically important. Also covered will be the FDA’s rights during the inspection and documentation you are not required to show them. WHY SHOULD YOU ATTEND FDA is required to conduct an inspection every two years. A company that is prepared for the inspection is less likely to receive 483’s than a disorganized company. If a 483 is received knowing how to respond will lessen chances of receiving an FDA warning letter. AREAS COVERED • Personnel preparation • Procedure to follow during FDA audits -what to do/ what not to do • Facility requirements to support FDA inspection • Behavior during inspection-what not to sign • Internal/ mock audits • 483s/ FDA Warning Letter response LEARNING OBJECTIVES Learn how to handle an FDA inspection efficiently. Also learn effective strategies to avoid 483s as well as for responding to an FDA warning letter. WHO WILL BENEFIT • Engineering personnel • Engineering management • Quality/ regulatory Management • Corporate Management • Manufacturing Management • Division management • Legal counsel For more detail please click on this below link: https://bit.ly/2xDpkDI Email: [email protected] Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882

How to prepare for and host an FDA inspection and respond to 483' will be held in Aurora,United States on date 2018-10-24

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Deadline for abstracts/proposals : 24th October 2018

Keynote Speakers : Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 9 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.

Venue :Training Doyens 26468 E Walker Dr,Aurora, Colorado

Check the event website for more details.