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Aug
8

FDA Inspection and Respond to 483 & How to Prepare them - 2017

 
 Conference CFP

When:

  08 Aug through 08 Aug 2017

CFP Deadline:

  08 Aug 2017

Where:

  Online Event | United States

Website URL:

  http://www.compliance4all.com/control/w_product/~product_id=501362LIVE?channel=brownwalker_Aug_2017_SEO

Sponsoring organization:

  Netzealous LLC DBA - Compliance4All

Categories:

  Education / Legal / Other - Education

Keywords:


Event description:

Overview: In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection. 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 a Warning Letter. Areas Covered in the Session: Personnel Preparation Facility needed to support inspection Behavior during inspection-what not to sign Internal/ Mock audits 483 response Who Will Benefit: Engineering Personnel Engineering Management Quality Management Corporate Management Manufacturing Management Division Management Speaker Profile: Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has... Read more

Posting date:

19 June 2017  |  181 views

Placement:

Not-featured (How do I make my event featured?)



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