2022年2022年计算机系统验证方案 .pdf
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1、SOP No./ 编号 : SOP01809/01 Page No./ 页码: Page 1 of 12 Any unauthorized use and copy is forbidden. 未经授权,不得使用或拷贝。Computerised System Validation 计算机系统验证Dept. 部门:Effective Date 生效日期:Confidential Level 机密等级: Top-secret 绝密 Confidential 机密 Cryptical 秘密Distribution List : 分发清单:QA 部、QC 部、OSP 固体制剂部、 Lo.物控部、 EN
2、 工程部、 TD 技术部、 EQ 设备部1 Objective 目的Role 责任人Draft 起草人Review 审核人Review 审核人Review 审核人Review 审核人Review 审核人Review 审核人Approve 批准人Dept. 部门QA QC OSP Lo. EN TD EQ QD Name 姓名Signature签名Date 日期Year/ 年Month/ 月QA 质量保证部Date/ 日名师资料总结 - - -精品资料欢迎下载 - - - - - - - - - - - - - - - - - - 名师精心整理 - - - - - - - 第 1 页,共 12
3、页 - - - - - - - - - Computerised System Validation 计算机系统验证Approve/ 批准人:SOP No./ 编号: SOP01809 /01 Date/ 日期:Page No./ 页码: Page 2 of 12 Test and assessment should be taken for URS, design, purchase, installation, function, as well as process adaptability of computerized and PLC control system related t
4、o GMP in compliance with this SOP so as to ensure that computerized and PLC are fit for design requirement and stated technical criteria and are able to work stably for a long time. 测试、评估采取的 URS、设计、采购、安装、功能以及计算机控制和PLC 控制系统符合 GMP,以确保计算机和PLC 符合设计要求和工艺要求并且能够稳定工作很长时间。2 Scope 范围This SOP is fit for the va
5、lidation management of computerized and PLC control system related to GMP, which apply to material control and management, laboratory equipment control and communication management, manufacturing process control, and utilities control. 本 SOP 适用于电脑 ,PLC 控制系统的管理是否符合GMP,物料控制和管理 ,实验设备控制和通信管理、生产过程控制、公用设施
6、的控制的验证。3 Responsibilities 职责QA is responsible for drafting, revising, reviewing, training, implementing and supervising this SOP. QA 负责起草、修订、审核、培训、实施和监督本SOP。The quality director is responsible for approving this SOP. 质量副总负责批准本SOP。Relevant departments are responsible for reviewing and implementing th
7、is SOP。相关部门负责审核和实施本SOP。4 Definitions定义Computerized or PLC control system: It composed of hardware, system software, applications, and relevant peripheral devices is a system that can implement a function and a set of functions. 无论是计算机化还是PLC 控制系统 :都是由硬件、系统软件、应用、及相关的周边设备组成的一个系统 ,可以实现某一功能和一套功能。Source c
8、ode: It is source program of computer whose format( program language) can be read by operator, before computer execution, it should be translate to machine language whose format can be executed by computer. 源代码:它是计算机的源程序 (程序语言 ),可以在电脑执行前被计算机识别,它应该被翻译成可以被计算机识别的机器语言。5 Procedures 程序5.1 5.1.1 5.1.2 Orga
9、nization of Validation team and responsibility 验证机构及责任Validation team is composed of supplier, QA, Equipment Department, use department. 验证团队由供应商 ,QA、工程设备部和使用部门组成。Implementation department responsibility of system validation 系统验证实施部门的职责Use department: Responsible for providing written URS, preparing
10、 validation protocol and report, implementing approved IQ and OQ protocol, completing final report and participating validation deviation investigation and alteration review. 名师资料总结 - - -精品资料欢迎下载 - - - - - - - - - - - - - - - - - - 名师精心整理 - - - - - - - 第 2 页,共 12 页 - - - - - - - - - Computerised Sys
11、tem Validation 计算机系统验证Approve/ 批准人:SOP No./ 编号: SOP01809 /01 Date/ 日期:Page No./ 页码: Page 3 of 12 使用部门 :负责提供书面的URS,准备验证方案和报告、实施批准IQ,OQ 协议,完成最终报告偏差并参与调查及变更验证审核。Equipment Department: Responsible for cooperating with use department to prepare URS and validation protocol, receiving system, installing sys
12、tem and implementing IQ, guiding use department on IQ and OQ process and participating validation deviation investigation and alteration review. 设备部门 :负责准备使用部门的合作协议,并确认你接收系统 ,安装系统 ,实施 IQ,指导使用部门关于 IQ 和 OQ 的验证过程和参与验证偏差调查和变更回顾。QA: Responsible for reviewing validation draft and final report, implementin
13、g validation protocol, participating validation deviation investigation and alteration approval and archiving validation protocol and report. QA:负责审查验证 ,也是最后一项报告草案、实施验证方案,参与调查及变更验证偏差的批准验证方案和归档,并做好报告。5.2 System classification 系统分级5.2.1 Before validation, evaluation and classification should be carrie
14、d out for system so as to insure that different grade validation should be provided for different type computerized and PLC control system. Classification as follows: 在验证之前 ,评估和分级应当进行系统分类,以确保不同等级验证需提供不同类型的计算机化的,PLC 控制系统 ,分类如下 : Classification 分类Description 描述Validation method 验证方法Operating system, n
15、etwork 网络操作系统 , Established network and operating system for commerce. E.g. DOSWindows 95/98NT. 已 做 好 网 络 和 操 作 系 统 例 如 :DOS Windows 95/98NT. Validate name and edition number 确认名称及版本号Standard device, microcontroller, sensitive equipment 标准配置 ,微控制器,灵敏的电气设备These system is designed by non-consumer for
16、driving firmware which can be installed in special integrate circuit (IC) for application, read only memory (ROM), random access memory (RAM), PLC sometimes, such as bar code modem, single-cycle controller, filling device, Checkweigher, temperature controller etc. 这些系统是根据用户可以安装在特殊的集成电路(IC)的驱动固件 ,只读存
17、储器 (ROM) 、随机存取存储器(RAM) 、PLC, 例如条形码调制解调器,single-cycle 控制器、灌装设备 ,重量控制、温度控制器等来设计的。Validate construction and configuration 确认构造及配置Standard package 标准程序包Ready-made package for commerce, such as multiplan software, standard chemical analysis software etc. 现成的软件包 ,例如多计划软件 ,标准化学分析软件等。Validate application pr
18、ocess 验证应用过程名师资料总结 - - -精品资料欢迎下载 - - - - - - - - - - - - - - - - - - 名师精心整理 - - - - - - - 第 3 页,共 12 页 - - - - - - - - - Computerised System Validation 计算机系统验证Approve/ 批准人:SOP No./ 编号: SOP01809 /01 Date/ 日期:Page No./ 页码: Page 4 of 12 Configurable package 可配置的程序包Users develop their own application th
19、rough pre-definite software modules and developing application modules can be carried out in this system, such as man-machine dialogue port, management control, data acquisition system, adaptive control system for laboratory, information management system for laboratory, material requirement plannin
20、g system, data processing system for system/ application and product, part PLC etc. 用户自己开发应用可通过pre-definite 软件模块和发展应用模块都可以在这个系统中运行,采用人机对话端口 ,管理控制 ,数据采集系统 ,自适应控制系统,信息管理系统 ,原材料需求计划系统、数据处理系统和产品、系统应用部分可编程序控制器(PLC)等。Audit supplier and validate application process and some pre-established code System deve
21、loped within firm 公司内部系统开发Modifying or developing system in compliance with requirement of himself 修改或开发符合自己要求的系统Implement all validation processes of computerized and PLC control system 实施计算机及PLC 控制系统验证的全过程5.2.2 Some computerized and PLC control system with complex construction should be classified
22、 in accordance with developing degree of each module. 一些计算机化的和 PLC 控制系统复杂程度应当跟各分类模块的开发程度相一致。5.2.3 Validation of computerized and PLC control system should be carried out not only for use process of system, e.g. validation of new system should be carried out not only for initial definition and design
23、ing phase but also whole life cycle of system development. 计算机验证 ,PLC 控制系统不仅体现在系统使用过程,如新系统的验证不仅在初始定义和设计阶段进行 ,而且贯穿于全部生命周期体系的发展。5.3 Validation implementation 验证实施5.3.1 URS URS should be prepared by system user and project expert detailed with fundamental requirement, expectation and performance index
24、of new/changed computerized and PLC control system, which will be use to determine system designing criteria. Content as follow: URS 应该为系统用户和项目专家准备基本要求详细的,预期和新的性能指标、 更改计算机化和 PLC 控制系统 ,可以用来决定系统设计标准。内容如下: 名师资料总结 - - -精品资料欢迎下载 - - - - - - - - - - - - - - - - - - 名师精心整理 - - - - - - - 第 4 页,共 12 页 - - -
25、- - - - - - Computerised System Validation 计算机系统验证Approve/ 批准人:SOP No./ 编号: SOP01809 /01 Date/ 日期:Page No./ 页码: Page 5 of 12 5.3.1.1 System description: what to do about system, how connection and interaction between different module, control methods (e.g. logic control, separation control, interloc
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