概述:描述清洁非洁净室区域的程序。适用于非洁净室区域，包括QC实验室、开发实验室、走廊、凉亭、储存区、办公室和办公桌区、休息室、洗手间、设备室等。包括:目的、范围、责任、参考和适用文件、材料和设备、健康和安全考虑、文件要求、，和程序包括附件/附录:非洁净室清洁记录表、清洁服务请求关于本文件: 这不是一个通用模板，它是一个6页的程序，实际上是在FDA监管机构的GMP操作中创建和使用的。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在做什么，哪些公司会从中受益: 制造经理材料控制人员质量控制人员

Summary:Describes procedures for cleaning the non-cleanroom areas. Applicable to non-cleanroom areas, including QC laboratories, development laboratories, corridors, coldrooms, storage areas, offices and desk areas, break rooms, restrooms, equipment rooms, etc.Included Sections:Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and ProceduresIncluded Attachments/Appendices:Non-Cleanroom Cleaning Logsheet, Janitorial Service RequestAbout This Document:This is not a generic template, it's a 6-page procedure that was actually created and used in the GMP 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:Manufacturing ManagersMaterial Control PersonnelQuality Control Personnel