翻譯后的計算機化系統(tǒng)驗證模板

1、Company LogoDOCUMENT NUMBER: # - #PAGE:1 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003Company LogoDOCUMENT NUMBER: # - #PAGE:2 of 56LOCATION: Revision: Rev #EF

2、FECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003Authors Signature:授權(quán)者簽名授權(quán)者簽名 Your signature indicates that this document has been prepared in accordance with existing project standards and adequ

3、ately reflects the tasks and deliverables necessary for validation of the 您的簽名表明這份文件的準備符合現(xiàn)行項目標準并且充分反映人物 u 和可交付使用對驗證的必要。Authored By:經(jīng)授權(quán)：經(jīng)授權(quán)：Typed/Printed Name, Title姓名，職稱Signature簽名Date日期Unit單位Reviewers Signature:審查員簽名：審查員簽名：Your signature indicates that, you have reviewed this document and that it a

4、ccurately and completely reflects the tasks and deliverables necessary for validation of the .您的簽名表明您已經(jīng)審閱了這份文件，確認它精確并完全的反映任務(wù)和可交付使用對驗證的必要。Reviewed By:經(jīng)審閱：經(jīng)審閱：Typed/Printed Name, Title姓名，職稱Signature簽名Date日期Unit單位Typed/Printed Name, Title姓名，職稱Signature簽名Date日期Unit單位Typed/Printed Name, Title姓名，職稱Signatu

5、re簽名Date日期Unit單位Quality Control/Compliance Approvers Signature:Company LogoDOCUMENT NUMBER: # - #PAGE:3 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003質(zhì)檢質(zhì)檢/承認簽名承

6、認簽名Your signature indicates that this document complies with ; and that the documentation and information contained herein complies with applicable regulatory, corporate, divisional/departmental requirements, and current Good Manufacturing Practices.您的簽名表明這份文件符合證明人驗證總計劃，企業(yè)標準或政策，并且在此包含的文件和信息符合可應(yīng)用的可調(diào)整

7、的，共同的以及部門所有的部門的要求和現(xiàn)行的標準。Approved By:經(jīng)核準：經(jīng)核準：Typed/Printed Name, Title姓名，職稱Signature簽名Date日期Unit單位Typed/Printed Na me, Title姓名，職稱Signature簽名Date日期Unit單位Company LogoDOCUMENT NUMBER: # - #PAGE:4 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad

8、7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003Revision History修訂歷史紀錄修訂歷史紀錄Revision修訂本修訂本Revision Date修訂日期修訂日期Reason for Revision/Change Request修訂修訂/更改要求的原因更改要求的原因Revised By修訂人修訂人004-DEC-20022002/12/4Original Release原始版本Michael T. Filary邁克爾116-JAN-20032003/1/16Updated

9、the JETT logo on the cover page.更新封頁面的 JETT 的標識Michael T. Filary邁克爾Table of Contents目錄1.Introduction 緒論.51.1Purpose 目的.51.2Policy Compliance 適用的政策 .51.3Scope of Validation 驗證范圍 .51.4Objectives 目標.61.5Periodic Review 定期審查 .62.Organizational Structure 組織結(jié)構(gòu).73.GxP Criticality AssessmentGxP 關(guān)鍵性評估.73.1Gx

10、P Criticality Assessment - RequirementsGxP 關(guān)鍵性評估要求.73.2GxP Criticality Assessment - Procedures GxP 關(guān)鍵性評估程序 83.3GxP Criticality Assessment Current StatusGxP 關(guān)鍵性評估現(xiàn)行標準.84.Validation Strategy 驗證策略.94.1Life Cycle 生命周期.94.2Risk Assessment 風(fēng)險評估.94.3Hardware Categories 硬件分類.94.4Software Categories 軟件分類.94.

11、5Project Inputs/Outputs for Stages 項目各階段的輸入/輸出.104.6Acceptance Criteria for Stages 各階段的接受標 10Company LogoDOCUMENT NUMBER: # - #PAGE:5 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Dat

12、e: 3/9/2216-1 月-20035.Validation Deliverables.105.1 Traceability and Linkages 描述和鏈接 115.2Master List of all Validation Products and Supporting Documentation所有批準產(chǎn)品和證明文件的總清單 115.3User Requirements Specification (URS) 使用說明書.115.4Functional Requirement Specification (FRS) 功能說明書.115.5Configuration Manage

13、ment and Change Control Documentation 配置管理和變速控制文件 115.6Vendor Qualification documentation 賣主資格認證 115.7Design Specifications 設(shè)計說明.125.8 Testing and Verification Requirements Documentation試驗和確認所需文件125.9System Security系統(tǒng)安全性.135.10Operational Support運行支持.145.11Business Continuity Plan業(yè)務(wù)持續(xù)計劃.145.12Disast

14、er Recovery, Backup and Restoration災(zāi)難性恢復(fù)，備份及修復(fù).145.13System Acceptance Final Report系統(tǒng)接受終報告.145.14列出任何其他需要驗證的產(chǎn)品.156.Acceptance Criteria可接受標準.157.Change Control變更控制.157.1Pre-Implementation Changes預(yù)執(zhí)行變更.157.2Post-Implementation Changes執(zhí)行后變更.158.Standard Operating Procedures SOP.158.1SOP Responsibilitie

15、s SOP 職責(zé).158.2Listing of SOPs SOP 列表.169.Training培訓(xùn).1610.Documentation Management資料管理.1610.1Document Production文件產(chǎn)生.1610.2Document Review文件回顧.1610.3Document Approval文件批準.1610.4Document Issue文件發(fā)布.1610.5Document Changes文件變更.1710.6Document Withdraw文件撤銷.1710.7Document Storage文件保存.1711.Maintaining the Va

16、lidated State驗證狀態(tài)的維護.1711.1System Retirement系統(tǒng)引退.1712.Validation Activities Timeline驗證執(zhí)行時間表.17Appendix A 附錄 A參與組織參與組織.18Appendix B 附錄 B縮寫詞，定義縮寫詞，定義.19Appendix C 附錄 C責(zé)任/時間.22Appendix D 附錄 D 可交付的驗證.23Company LogoDOCUMENT NUMBER: # - #PAGE:6 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VAL

17、IDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003Appendix E 附錄 E 參考.24(Reminder of Page Intentionally Left Blank)Company LogoDOCUMENT NUMBER: # - #PAGE:7 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION P

18、LAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-20031. Introduction緒論1.1 Purpose 目的This document, also referred to as the Plan, outlines the planned tasks and expectations for validation of the .這份文件，也稱計劃，略述計劃的任務(wù)和設(shè)備名稱的預(yù)期驗證。WHO will be r

19、esponsible for completion, review, and approval of these tasks.世界衛(wèi)生組織將負責(zé)任務(wù)的完成、審閱和批準。世界衛(wèi)生組織將負責(zé)任務(wù)的完成、審閱和批準。WHAT documentation/deliverables will be generated and/or retained as part of the Validation Package(s).什么文件/可交付使用的將會作為驗證包的一部分被產(chǎn)生和/或保留。HOW this documentation will be produced/created (at a macro l

20、evel).這份文件將被如何制作這份文件將被如何制作/產(chǎn)生（在宏觀上）。產(chǎn)生（在宏觀上）。1.2 Policy Compliance遵守政策This Plan is being written to comply with corporate policy requirements for validation as stated in the , and the appropriate Appendix of the current revision of GAMP.這份計劃將會遵守在涉及特殊驗證總計劃，公司政策，公司標準和公司指導(dǎo)方針和適當(dāng)性（現(xiàn)行 GAM附錄）中關(guān)于驗證的統(tǒng)一要求。The

21、 validation of the system is a cGMP requirement. 設(shè)備名稱的驗證系統(tǒng)是現(xiàn)行的一個要求。1.3 Scope of Validation驗證范圍This Validation Plan for the is limited to the unique components and control system that define the equipment. This validation effort will be conducted as a prospective validation.這份為設(shè)備名稱的驗證計劃僅限于特殊構(gòu)成和定義設(shè)備的控

22、制系統(tǒng)。該項驗證成就將會被作為一項預(yù)期的驗證執(zhí)行。Provide a Brief description of equipment and principal function; Refer to User Requirement Specifications. Provide a description of the research, manufacturing, processing, packaging, holding, or distribution process for which the equipment is planned.對用戶必備使用的說明書中的設(shè)備和主要功能的闡述

23、. 對實施計劃的設(shè)備進行研究、生產(chǎn)、加工、包裝、存儲、分配過程的說明。Company LogoDOCUMENT NUMBER: # - #PAGE:8 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-20031.3.1 In-Scope驗證范圍The scope of validat

24、ion for the includes all the following that are necessary for the system to operate. （設(shè)備名稱）驗證的范圍包括以下所有的系統(tǒng)運作所必需的內(nèi)容。（明確界限）1.Controls system hardware and software控制系統(tǒng)得硬件和軟件2.Mechanical Hardware機械的硬件3.Instrumentation儀器4.Process piping輸水管道工藝5.Utility Systems通用系統(tǒng)6.Facility設(shè)施7.其他需要的名單1.3.2 Out-of-Scope驗證范圍

25、例外The scope of validation for the does not include:（設(shè)備名稱）驗證的范圍不包括：1.The XYZ system is validated separately.系統(tǒng)單獨驗證2.The Data Historian is validated separately.數(shù)據(jù)歷史單獨驗證3.其他名單Company LogoDOCUMENT NUMBER: # - #PAGE:9 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File

26、Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-20031.3.3 Related Validation相關(guān)驗證插入現(xiàn)有的或計劃的與本驗證系統(tǒng)有關(guān)的驗證的描述。如果系統(tǒng)配置和數(shù)據(jù)采集時是一致的，前期數(shù)據(jù)的使用可以作為試驗方法的參考或直接替代試驗，The related validation that will occur in support of the includes all the following that are necessary for

27、 the system to be placed into operation. 支持（設(shè)備名稱）的相關(guān)驗證在以下情況發(fā)生：包括系統(tǒng)運行必需的幾點（清晰的定義分界線）：1.Process Validation工藝驗證2.Cleaning Studies清潔研究3.Air Classification風(fēng)力分級4.Microbiological Testing微生物試驗5.Chemical Testing化學(xué)試驗6.Drying Studies干燥研究7.Sterilization Studies無菌研究8.其他名單1.4 Objectives目標The objective of this val

28、idation plan is to outline the requirements that will demonstrate and document that all components, control system(s) and functionality associated with the are appropriate Company LogoDOCUMENT NUMBER: # - #PAGE:10 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File

29、 Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003for cGMP-regulated processes. The qualifications outlined are to be based on policies and procedures and applicable regulations, guidelines, and accepted industry practices for validation.該項驗證計劃的目標是簡述

30、一項要求，該要求能夠證明所有與設(shè)備名稱相關(guān)的組成、控制系統(tǒng)和功能都是恰當(dāng)?shù)姆犀F(xiàn)行標準的工藝。資格的綜述要基于（公司名稱）政策，程序以及可應(yīng)用的規(guī)則、指導(dǎo)方針和公認的工業(yè)驗證實踐。1.5 Periodic Review定期回顧This Plan should be reviewed periodically to ensure compliance and or to determine if a change is required. Some appropriate times to review are:這份計劃應(yīng)該被定期回顧來保證符合并確定是否需要更改。一些適當(dāng)?shù)幕仡檿r間是：1. Ch

31、ange in Validation Master Plan驗證主文件的更改發(fā)生時2. Change in scope occurs驗證范圍的更改發(fā)生時3. Design change occurs設(shè)計更改發(fā)生時4. Prior to IQ and OQ在進行和之前5. Completion of IQ and OQ和完成時See section 5 for a description of Validation Management and the process for review and revisions to this plan or refer to the applicable

32、 corporate policy review cycle.見第五部分有關(guān)驗證管理和針對該項計劃見第五部分有關(guān)驗證管理和針對該項計劃 的回顧、修訂過程或指適應(yīng)公司政策的回顧周期。的回顧、修訂過程或指適應(yīng)公司政策的回顧周期。2. Organizational Structure組織結(jié)構(gòu)Specific responsibilities related to the validation of the are outlined in Appendix A. In general, the activities associated with this project, are the respo

33、nsibility of the following individuals and groups:與（設(shè)備名稱）驗證相關(guān)的具體職責(zé)在附錄中概述。大體上，與驗證相關(guān)的活動項目由以下個人和部門負責(zé)：確定個人的任務(wù)和責(zé)任至少應(yīng)包括以下幾點，總體根據(jù)崗位不同描述每項任務(wù)和責(zé)任1.Management level Responsible for project management and planning, control of project activities/resources/costs, monitoring process, initiating corrective action,

34、ensuring issues/project objectives are correctly addressed/resolved, reporting to senior management, interface to QA to ensure compliance, reviewing and approving validation documentation for the project管理層：負責(zé)項目管理和計劃。方案，活動，資源，成本的控制，監(jiān)控工藝，2.Quality Assurance Responsible for assuring compliance with ap

35、propriate Company LogoDOCUMENT NUMBER: # - #PAGE:11 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003regulatory/business/technical/user community requirements, pro

36、viding support for the criterion/independent review/approval of deliverables, approving completion of stage/validation status質(zhì)保：負責(zé)保證符合適當(dāng)?shù)恼{(diào)整、商業(yè)、技術(shù)、用戶群要求，支持維護標準、獨立審查、可交付的批準、審批完成階段和身份驗證等。3.System Owner Responsible for implementation/management of the system by the business user community, approving com

37、pletion of stage/validation status系統(tǒng)所有者：負責(zé)執(zhí)行和管理系統(tǒng)的用戶群，審批完成階段和驗證身份。這些任務(wù)和責(zé)任可以適當(dāng)?shù)亩x：按照他們的分工總體上定義每項任務(wù)和責(zé)任。1.Operations Responsible for providing操作：負責(zé)提供2.Project Level Responsible for providing項目水平：負責(zé)提供3.Technical and Engineering support Responsible for providing技術(shù)和工程支持：負責(zé)提供4.Validation Specialist Respons

38、ible for providing驗證專家：負責(zé)提供5.System Administrator Responsible for providing系統(tǒng)管理：負責(zé)提供6.Purchasing - Responsible for providing采供：負責(zé)提供7.其他名單3.GxP Criticality AssessmentGxP 關(guān)鍵性估計Detail the GxP criticality assessment information related to the . This section may reference another source of information co

39、vering this topic, such as a system inventory.詳述和（設(shè)備名稱）有關(guān)的 GxP 關(guān)鍵性估計信息。該部分包括另外一種信息，包括該主題，例如系統(tǒng)詳細目錄。 Company LogoDOCUMENT NUMBER: # - #PAGE:12 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Pr

40、int Date: 3/9/2216-1 月-20033.1GxP Criticality Assessment RequirementsGxP 關(guān)鍵性評估要求Define the requirements used in the determination of the levels for GxP criticality for the . The requirements for determination of the levels for GxP criticality may include Direct Impact, Indirect Impact, and No Impact

41、 systems.定義在決定（設(shè)備名稱）Gxp水平中使用的關(guān)鍵性要求，包括直接影響，間接影響和無影響系統(tǒng)。Direct Impact System or component within a system where the operation, contact, data, control, alarm, or failure will have a direct impact on product quality.直接影響：系統(tǒng)或系統(tǒng)中的一個組成，對產(chǎn)品質(zhì)量有直接影響的操作，接觸，控制，預(yù)警或失敗。Indirect Impact System or component within a s

42、ystem where the operation, contact, data, control, alarm, or failure will not have a direct impact on product quality. Indirect Impact systems typically support Direct Impact systems, thus indirect impact system may have an affect on the performance or operation of a direct impact system.間接影響：系統(tǒng)或系統(tǒng)中

43、的一個組成，對產(chǎn)品質(zhì)量無直接影響的操作，接觸，控制，預(yù)警或失敗。間接影響系統(tǒng)專門支持直接影響系統(tǒng)，因此間接影響系統(tǒng)會對直接影響系統(tǒng)的執(zhí)行和運作構(gòu)成影響。No Impact System or component within a system where the operation, contact, data, control, alarm, or failure will not have a direct or indirect impact on product quality. No Impact systems will not support Direct Impact syst

44、ems.無影響：系統(tǒng)或系統(tǒng)的一個組成，對產(chǎn)品質(zhì)量不構(gòu)成直接或間接影響的操作，接觸，控制，預(yù)警或失敗。無影響系統(tǒng)不能支持直接影響系統(tǒng)。3.2GxP Criticality Assessment ProceduresGxP 關(guān)鍵性評估-程序Define the procedures used/followed in the assessment of the levels for GxP criticality for the . Develop a documented path that will be followed to determine the levels for GxP crit

45、icality for each item associated with the . It may be helpful to develop a decision tree to demonstrate the overview to the process required in determining levels for GxP criticality. Internal procedures may be referenced, if available.定義使用的程序/（設(shè)備名稱）的 Gxp 關(guān)鍵性水平的評估的標準。開發(fā)一種具有證明的文件路徑，作為（設(shè)備名稱）GxP 關(guān)鍵性水平每

46、一項目的評估標準。創(chuàng)建一個決策樹將對在 GxP 關(guān)鍵性評估中論證工藝的一般觀察要求有幫助。如果必要，可以引用國際程序作為參考。3.3GxP Criticality Assessment Current StatusGxP 關(guān)鍵性評估-現(xiàn)行標準State the current status of the assessment for the GxP criticality levels for the . 陳述現(xiàn)行（設(shè)備名稱）的 GxP 關(guān)鍵性水平評估的要求。Company LogoDOCUMENT NUMBER: # - #PAGE:13 of 56LOCATION: Revision: R

47、ev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003The Direct Impact Systems associated with the include all the following. （設(shè)備名稱的）直接影響因素包括以下的所有項。（清楚的規(guī)定支持理論）1.Controls system hardware and sof

48、tware - This has been deemed a direct impact system due to控制系統(tǒng)硬件和軟件：該項是一個直接影響由于2.Mechanical Hardware - This has been deemed a direct impact system due to機械硬件：該項是一個直接影響由于3.Instrumentation This has been deemed a direct impact system due to儀器：該項是一個直接影響由于4.Process piping - This has been deemed a direct

49、impact system due to工藝流程：該項是一個直接影響由于5.Utility Systems - This has been deemed a direct impact system due to效用系統(tǒng)：該項是一個直接影響由于6.Facility - This has been deemed a direct impact system due to設(shè)備：該項是一個直接影響由于7.其他名單The Indirect Impact Systems associated with the include all the following. （設(shè)備名稱的）間接影響因素包括以下的所有

50、項。（清楚的規(guī)定支持原理）1.Controls system hardware and software - This has been deemed an indirect impact system due to控制系統(tǒng)硬件和軟件：該項是一個間接影響由于2.Mechanical Hardware - This has been deemed an indirect impact system due to機械硬件：該項是一個間接影響由于3.Instrumentation This has been deemed an indirect impact system due to儀器：該項是一

51、個間接影響由于4.Process piping - This has been deemed an indirect impact system due toCompany LogoDOCUMENT NUMBER: # - #PAGE:14 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1

52、 月-2003工藝流程：該項是一個間接影響由于5.Utility Systems - This has been deemed an indirect impact system due to效用系統(tǒng)：該項是一個間接影響由于6.Facility - This has been deemed an indirect impact system due to設(shè)備：該項是一個間接影響由于7.其他名單The No Impact Systems associated with the include all the following. （設(shè)備名稱的）無影響因素包括以下的所有項。（清楚的規(guī)定支持原理）

53、1.Controls system hardware and software - This has been deemed a no impact system due to控制系統(tǒng)硬件和軟件：該項是一個無影響系統(tǒng)由于2.Mechanical Hardware - This has been deemed a no impact system due to機械硬件：該項是一個無影響系統(tǒng)由于3.Instrumentation This has been deemed a no impact system due to儀器：該項是一個無影響系統(tǒng)由于4.Utility Systems - This

54、 has been deemed a no impact system due to工藝流程：該項是一個無影響系統(tǒng)由于5.Facility - This has been deemed a no impact system due to設(shè)備：該項是一個無影響系統(tǒng)由于6.其他名單4.Validation Strategy驗證策略4.1Life Cycle生命周期Company LogoDOCUMENT NUMBER: # - #PAGE:15 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR

55、 THE File Name: eedad5e326d5dad7a0a283f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003Define the internal requirements for development, testing, delivery, and support that define the period of time that begins when a system is conceived and ends when the system is no longer av

56、ailable for use.陳述國內(nèi)研發(fā)，測試，運輸和維護的要求，定義驗證開始的時間段（系統(tǒng)存在時開始），系統(tǒng)結(jié)束的時間（系統(tǒng)不可用時結(jié)束）。4.2Risk Assessment風(fēng)險評估State the current status of the assessment for the GxP Risk and Business Risk for the . The process needs to address the following questions:陳述現(xiàn)行（設(shè)備名稱）的 GxP 關(guān)鍵性水平評估的風(fēng)險和商業(yè)風(fēng)險。該程序必須包括以下問題：Does this automated

57、system require validation?自動化系統(tǒng)需要驗證嗎？How much validation is required for this system?該系統(tǒng)要求多少驗證？What aspects of the system or process are critical to product and patient safety?系統(tǒng)的哪個方面或工藝對產(chǎn)品和患者安全性是關(guān)鍵性因素？What aspects of the system or process are critical to business?系統(tǒng)的哪個方面或工藝過程對商業(yè)是關(guān)鍵性因素?4.3Hardware C

58、ategories硬件分類Define the categories of the hardware associated with the . 定義(設(shè)備名稱)的硬件種類Hardware components of a system can be analyzed and categorized into one of the following GAMP defined categories:硬件系統(tǒng)組成可以按照以下GAMP詳述的分類方法進行分析和歸類：Hardware Category 1 Standard Hardware Components硬件分類1: 標準硬件組成 Hardwar

59、e Category 2 Custom Built Hardware Components硬件分類2：定制的硬件組成4.4Software Categories軟件分類Define the categories of the software associated with the . Company LogoDOCUMENT NUMBER: # - #PAGE:16 of 56LOCATION: Revision: Rev #EFFECTIVE: yyyy.mm.ddTITLE: VALIDATION PLAN FOR THE File Name: eedad5e326d5dad7a0a28

60、3f769fd49ff.pdfCLast Save Date: 02-9 月-2011Print Date: 3/9/2216-1 月-2003定義(設(shè)備名稱)的軟件種類Software components of a system can be analyzed and categorized into one of the following GAMP defined categories:軟件系統(tǒng)組成可以按照以下GAMP詳述的分類方法進行分析和歸類：Software Category 1 Operating Systems軟件分類1：運行系統(tǒng)Software Category 2 Fir