Full Description

Summary:

Describes the procedure for maintaining the controlled external document file. Includes provisions for international and domestic regulations and standards applicable to product design, quality systems, manufacturing operations, and compliance with 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 2-page procedure that was actually created and used in the Document Control 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:

Document Control PersonnelConfiguration ManagementQuality Assurance Managers

Product Details:

Edition: 1.0 Published: 08/01/2007 Number of Pages: 2