摘要:旨在确保正确接收、登录和跟踪提交给实验室进行免疫细胞化学分析的人类样本。适用于接收、登录和以其他方式处理生物样本的所有实验室人员。包括接收冷冻样本、石蜡包埋样本和血液制品样本的说明。包括的章节:目的、范围、责任、参考文件和适用文件、材料和设备、健康和安全注意事项、文件要求和程序包括的附件/附录:无关于本文件:这不是一个通用模板，它是一个三页的程序，实际上是在FDA的实验室研发操作中创建和使用的- 受监管的机构。公司特定信息（名称、地址、一些图片、专有产品信息等）已被编辑，但内容和格式已基本保留。购买理由:将其作为你自己文档项目的起点，将你文档的质量与你所在行业的同行进行比较，了解你所在行业的其他公司实际在做什么，谁将从中受益:流程开发人员方法开发人员质量控制人员

Summary:Intended to assure the proper receipt, log-in, and tracking of human specimens submitted to the laboratory for immunocytochemical analysis. Applies to all laboratory personnel who receive, log-in and otherwise handle biologic specimens. Includes instructions for receiving frozen samples, paraffin-embedded specimens, and blood product specimens.Included Sections:Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and ProceduresIncluded Attachments/Appendices:NoneAbout 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 projectCompare the quality of your documents against your industry peersLearn what other companies in your industry are actually doingWho Will Benefit:Process Development PersonnelMethod Development PersonnelQuality Control Personnel