概述:描述如何确保所有在制品（WIP）材料的正确发放、接收、处理、储存，以及批次跟踪，以防止损坏、混淆、污染或其他不利影响。适用于支持生产的所有在制品（WIP）材料。包括一般程序、向WIP分配材料、WIP材料的退货和接收、成品处理。设计用于MRP数据库，但可以轻松适应其他类型的库存系统。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附件/附录:关于本文件:这不是一个通用模板，它是一个4页的程序，实际上是在FDA监管机构的材料控制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，谁会从中受益:材料控制人员制造经理质量保证经理

Summary:Describes how to ensure the proper issuing, receiving, handling, storage of all work in process (WIP) materials, and lot tracking to prevent damage, mix-up, contamination, or other adverse effects. Applies to all work in process (WIP) materials in support of production. Includes general procedures, distribution of material to WIP, return and receipt of WIP materials, finished goods handling. Designed for use with an MRP database but could easily be adapted for other types of inventory systems.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 4-page procedure that was actually created and used in the Material Control 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:Material Control PersonnelManufacturing ManagersQuality Assurance Managers