Engineering Change Control

This webinar will outline a system for efficient change control, focusing on regulations and practical experience, explaining pre-release and post-release control, methods for transfer and approval, and detailed change control forms.

Edwin Waldbusser
Instructor:
Edwin Waldbusser
Date:
Friday, May 10, 2024
Time:
10:00 AM PDT | 01:00 PM EDT
Duration:
60 Minutes

More Trainings by this Expert   Product Id : 505940

Price Details
$150 Live
$290 Corporate Live
$190 Recorded
$390 Corporate Recorded
Combo Offers
Live + Recorded
$289 $340 Live + Recorded
Corporate (Live + Recorded)
$599 $680 Corporate
(Live + Recorded)
Price Detail Options
Overview:

This webinar will describe a system, based on the regulations and practical experience that will allow for efficient control of the change process.

It will be compliant but not cumbersome or overly time consuming. The difference between pre release and post release change control will be explained. Methods to control the transfer and approval of changes between the company and its suppliers or contract manufacturers will be explained. Change control forms will be provided and described in detail.

Why should you Attend: FDA and ISO require change control but do not provide any further guidance as to how to create a compliant system. The situation gets complicated when a company has suppliers or contract manufacturers and changes and approvals must pass from one to the other. This webinar will describe a system, based on the regulations and years of practical experience that will allow for efficient control of the change process. It will be compliant but not cumbersome or overly time consuming. Change control forms will be provided and explained.

Areas Covered in the Session:

  • Why change control Change control procedure Pre release and post release change control Evaluating impacts on WIP, tooling,etc
  • Change transfer between company and suppliers Forms and SOP’s

Who Will Benefit:
  • Development Engineers
  • Production Management
  • QA/ QC Personnel
  • Engineering Management
  • Regulatory Personnel


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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