Description
Summary:
Provides a system for identifying and tracking major Quality Improvement Projects (QIP). Applies to existing or new corrective action projects that will require substantial company resources and/or time to complete. Includes provisions for project identification and assignment, project plan development, project approval, tracking and status, project completion and documentation requirements.
Included Sections:
Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and Procedures
Included Attachments/Appendices:
Quality Improvement Project Description Form, Example of Completed Description Form
About This Document:
This is not a generic template, it's a 5-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 project
- Compare the quality of your documents against your industry peers
- Learn what other companies in your industry are actually doing
Who Will Benefit:
- Quality Assurance Managers
- Manufacturing Managers
- Regulatory Affiars Managers
Product Details
- Edition:
- 1.0
- Published:
- 08/01/2007
- Number of Pages:
- 5
- File Size:
- 1 file , 2.8 MB
