How to Prepare for and Host an FDA Inspection and respond to 483's

Edwin Waldbusser
Duration: 60 Minutes
Webinar Id: 603392
Instructor: Edwin Waldbusser

Price Details

Recorded Webinar
$190. One Attendee
$390. Unlimited Attendees

Unlimited Attendees: Any number of participants

Recorded Version: Unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of live webinar)

Overview:

In this webinar you will learn how to prepare for an inspection and how to respond to a 483 or Warning letter if you receive one.

You will learn about the types of FDA inspections, preparations such as assigning personnel to specific tasks for the 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 how to respond 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 you should Attend:

FDA will inspect you! Are you ready? 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 the chances of receiving a Warning Letter.

The handout is inspection readiness checklist

Areas Covered in the Session:

  • Personnel Preparation
  • Procedure to follow during audit-what to do/ what not to do
  • Facility Requirements to support Inspection
  • Behavior during inspection-what not to sign
  • Internal/ Mock Audits
  • 483/ Warning Letter response

Who Will Benefit:

  • Engineering Personnel
  • Engineering Management
  • Quality/ Regulatory Management
  • Corporate Management
  • Manufacturing Management
  • Division Management
  • Legal Counsel

Speaker Profile
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 8 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.

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