Description
Summary:
Describes a procedure to assure proper quality control of all reagents and instrumentation that are used in immunocytochemical procedures performed in this laboratory. Applies to all laboratory personnel who process, immunostain, or interpret the results of patient specimens. Includes provisions for specimen processing requests, fixatives, Ficol-Hypaque, buffer solutions, immunostaining kits/reagents, laboratory instrumentation, tissue culture incubators, biological safety cabinets, centrifuges, and cytocentrifuges.
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 Laboratory R&D 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:
- Process Development Personnel
- Method Development Personnel
- Quality Control Personnel
Product Details
- Edition:
- 2.0
- Published:
- 08/01/2007
- Number of Pages:
- 3
- File Size:
- 1 file , 290 KB
