Description
Summary:
Provides procedures for the calibration of instruments by approved vendors, both on-site or off-site. Applicable to automatic, mechanical and electronic equipment used in development, production, environmental control, and testing for products. Suitable for Manufacturing, Facilities, Product Engineering, and QA/QC. Includes provisions for handwritten data entries, calibration certificates, and scheduling and requisitioning.
Included Sections:
Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and Procedures
Included Attachments/Appendices:
Instrument Shipping Form
About This Document:
This is not a generic template, it's a 5-page procedure that was actually created and used in the Facilities & Equipment 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:
- Manufacturing Personnel
- Facilities Managers
- Laboratory Personnel
Product Details
- Edition:
- 1.0
- Published:
- 08/01/2007
- Number of Pages:
- 5
- File Size:
- 1 file , 340 KB
