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Medical Device Single Audit Program (MDSAP) QUALITY MANAGEMENT SYSTEM MANUAL

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发表于 2017-9-21 15:32:08 | 显示全部楼层 |阅读模式
Table of Contents
Introduction ........... 5
1. Scope ............ 6
2. Normative References ........... 8
3. Terms and Definitions............ 9
4. Context of MDSAP..................12
4.1 Understanding MDSAP and its context..............12
4.2 Needs and expectations of interested parties....12
4.3 Scope of the quality management system.........13
4.4 Quality management system and its processes.............13
5. Leadership...............14
5.1 Leadership and Commitment..... 14
5.1.1 General...........14
5.1.2 Customer Focus .........15
5.2 Policy .................15
5.3 Organizational roles, responsibilities and authorities .....16
6. Planning..........18
6.1 Actions to address risks and opportunities ............18
6.2 Quality Objectives and planning to achieve them..............18
6.3 Planning of changes..........18
7. Support ........20
7.1 Resources ............. 20
7.1.1 General...........20
7.1.2 People............. 20
7.1.3 Infrastructure...............21
7.1.4 Environment for the operation of processes ...21
7.1.5 Monitoring and measuring resources..............21
7.1.6 Organizational knowledge.......21
7.2 Competence..........21
7.3 Awareness............. 22
7.4 Communication .................22
7.5 Documented information ...............22
7.5.1 General...........22
7.5.2 Creating and updating ............24
7.5.3 Control of documented information.....24
8. Operation ........26
8.1 Operational planning and control ...........26
8.2 Requirements for products and services ...........27
8.2.1 Customer communication .......27
8.2.2 Determining the requirements for products and services........27Review of the requirements for products and services ...........27
8.2.4 Changes to requirements for products and services...28
8.3 Design and Development of products and services.......28
8.3.1 General...........28
8.3.2 Design and development planning......28
8.3.3 Design and development inputs..........29
8.3.4 Design and development controls.......29
8.3.5 Design and development outputs .......30
8.3.6 Design and development changes......30
8.4 Control of externally provided processes, products and services ..........31
8.4.1 General...........31
8.4.2 Type and extent of control ......31
8.4.3 Information for external providers .......31
8.5 Production and Service Provision ..........31
8.5.1 Control of Production and Service Provision...31
8.5.2 Identification and Traceability .............32
8.5.3 Property belonging to customers or external providers...........32
8.5.4 Preservation................33
8.5.5 Post-delivery activities ............33
8.5.6 Control of changes......33
8.6 Release of products and services..........33
8.7 Control of nonconforming outputs..........33
9. Performance evaluation ..........35
9.1 Monitoring, measurement, analysis and evaluation.......35
9.1.1 General...........35
9.1.2 Customer satisfaction .............36
9.1.3 Analysis and evaluation ..........36
9.2 Internal Audit .........36
9.3 Management review..........37
9.3.1 General...........37
9.3.2 Management review inputs..... 38
9.3.3 Management review outputs...............38
10. Improvement ............. 39
10.1 General................39
10.2 Nonconformity and corrective action .......39
10.3 Continual Improvement ...............39

Medical Device Single Audit Program (MDSAP) QUALITY MANAGEMENT SYSTEM MANUAL.rar

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发表于 2017-9-21 17:15:47 | 显示全部楼层

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 楼主| 发表于 2017-9-21 19:03:20 | 显示全部楼层

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发表于 2017-9-22 08:04:32 | 显示全部楼层
谢谢分享。。。

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 楼主| 发表于 2017-9-22 11:34:50 | 显示全部楼层
billye 发表于 2017-9-22 08:04
谢谢分享。。。

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 楼主| 发表于 2017-9-22 11:35:19 | 显示全部楼层

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 楼主| 发表于 2017-9-22 12:12:36 | 显示全部楼层

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发表于 2017-9-23 11:49:25 | 显示全部楼层

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发表于 2017-9-26 14:46:32 | 显示全部楼层
Is it also high level structure for medical product?

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发表于 2022-12-16 14:54:14 | 显示全部楼层
感谢分享
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