Full Description

Summary:

Describes the general requirements for inspection and testing of manufactured materials. Applies to raw materials, sub-assemblies, final products, and finished goods manufactured by and for GMP production of devices, drugs, and biologics.

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 Quality Assurance 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:

Quality Assurance ManagersManufacturing ManagersMaterial Control Personnel

Product Details:

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