ENGINEERING CONTROL CHANGE IN MEDICAL DEVICES
🎤 Edwin Waldbusser | 📅 May 24, 2023 | 🕒 11 AM Eastern Time US
Description:
Change control focuses on managing changes throughout a product’s life cycle as a part of current good manufacturing practices. Extensive regulations ensure that changes don’t put the safety, reliability and performance of products at risk. Therefore, it’s critical that medical device manufacturers adhere to all of the regulatory change control guidelines.
FDA and ISO call for 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 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.
AREAS COVERED IN THE SESSION:
- What is an engineering change order?
- Change control procedure
- Pre release and post release change control
- Change transfer between company and suppliers
- Forms and SOP's.
WHO SHOULD ATTEND:
- Quality Assurance Departments
- Quality Control Departments
- Regulatory Affairs Departments
- Manufacturing Departments
- Engineering Departments
- Production Departments
- Development Engineers
