Description
Summary:
Describes the procedure for determining which changes to the Quality System and/or Product Design need further approval from the Notified Body prior to implementation. Intended to explain the strategy towards voluntary notification of changes that do not require further approval of the Notified Body but that are nevertheless notified because of their importance. Applies to all planned changes to approved Quality System and/or approved Product Design of a CE marked medical devices regulated by the Medical Device directive (93/42/EEC).
Included Sections:
Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and Procedures
Included Attachments/Appendices:
None
About This Document:
This is not a generic template, it's a 2-page procedure that was actually created and used in the Regulatory Affairs operations of a FDA-regulated establishment. The company-specific information (names, addresses, some images, proprietary product information, etc.) has been redacted but the content and format have been largely preserved.
Reasons to Buy:
- Use it as a starting point for your own documentation project
- Compare the quality of your documents against your industry peers
- Learn what other companies in your industry are actually doing
Who Will Benefit:
- Regulatory Affairs Managers
- Management Representatives
- Executive Management
Product Details
- Edition:
- 2.0
- Published:
- 08/01/2007
- Number of Pages:
- 2
- File Size:
- 1 file , 270 KB
