Full Description

Summary:

Provides a guideline for establishing the content of a product design review and a guideline for conducting and documenting design reviews. Intended for all design controlled projects being tracked under a project management system. Covers general design review process and review requirements, and includes provisions for compliance ISO 9001.

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 3-page procedure that was actually created and used in the Device Engineering 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 projectCompare the quality of your documents against your industry peersLearn what other companies in your industry are actually doing

Who Will Benefit:

Engineering ManagersQuality Assurance ManagersEngineering Development & Manufacturing Personnel

Product Details:

Edition: 1.0 Published: 08/01/2007 Number of Pages: 3