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BSI 22/30461479 DC:2022 Edition

BSI 22/30461479 DC:2022 Edition

$13.70

BS ISO 27025. Space systems. Programme management. Quality assurance requirements

Published By Publication Date Number of Pages
BSI 2022 61
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PDF Catalog

PDF Pages PDF Title
1 30461479-NC.pdf
3 ISO_DIS 27025 ed.2 – id.85522 Enquiry PDF (en) (2).pdf
9 Foreword
10 Introduction
11 1 Scope
2 Normative references
3 Terms, definitions and abbreviated terms
3.1 Terms and definitions
12 3.2 Abbreviated terms
3.2.1 General
3.2.2 Abbreviated terms relating to document requirement definition
13 4 QA programme management
4.1 QA programme
14 4.2 Organization
4.3 QA programme plan
4.4 QA status reporting
4.5 Personnel training and certification
15 4.6 QA programme audits
4.7 QA role in configuration management
4.8 Critical items control
16 5 Quality assurance general requirements
5.1 Documentation and data control
5.2 Records
17 5.3 Stamp control
5.4 Traceability
5.4.1 General
5.4.2 Identification
18 5.4.3 Data retrieval system
5.5 Metrology and calibration
19 5.6 Nonconformance control system
21 5.7 Alert system
5.7.1 Supplier participation
5.7.2 PA experts involvement
5.7.3 Generation of alerts within the project
5.7.4 Processing of alerts from other sources
22 5.8 Handling, storage and preservation
5.8.1 Handling
5.8.2 Storage
5.8.3 Preservation
5.9 Statistical quality control and analysis
5.9.1 General
5.9.2 Sampling plans
23 6 QA requirements for design and verification
6.1 General
6.2 Planning
6.3 Organizational and technical interfaces
24 6.4 Design rules
6.4.1 General
6.4.2 Producibility
6.4.3 Repeatability
25 6.4.4 Inspectability and testability
6.4.5 Operability
6.5 Standards and procedures
6.5.1 General
6.5.2 Provisions
26 6.6 Verification
6.6.1 General
6.6.2 Design verification analysis
6.6.3 Design reviews
27 6.6.4 Qualification process
28 6.7 Design changes
7 QA requirements for procurement
7.1 General
7.2 Selection of procurement sources
7.2.1 General
7.2.2 Selection criteria
7.2.3 Record and list of procurement sources
29 7.3 Procurement documents
7.3.1 General
7.3.2 Procurement documents
7.3.3 Review of procurement documents
7.3.4 Product assurance documentation to deliver
7.4 Surveillance of procurement sources
7.4.1 General
7.4.2 Surveillance programme
30 7.4.3 Criteria for surveillance
7.4.4 Surveillance of lower level suppliers
7.5 Receiving inspection
7.5.1 General
7.5.2 Receiving inspection activities
31 7.5.3 Customer furnished items
7.5.4 Receiving inspection records
8 QA requirements for manufacturing, assembly and integration
8.1 General
8.2 Planning of manufacturing, assembly and integration activities and associated documents
32 8.3 Manufacturing readiness reviews
8.3.1 General
8.3.2 Objectives
33 8.4 Control of processes
8.4.1 General
8.4.2 Critical processes
8.4.3 Statistical process control
8.5 Workmanship standards
8.5.1 General
34 8.5.2 Identification of criteria
8.5.3 Samples
8.6 Materials and parts control
8.6.1 General
8.6.2 Items marks
8.6.3 Sensitive items
8.7 Equipment control
8.7.1 Tools
8.7.2 Equipment for computer-aided manufacturing
35 8.8 Cleanliness and contamination control
8.8.1 General
8.8.2 Cleanliness levels
8.8.3 Cleaning materials and methods
8.8.4 Contamination control
8.8.5 Cleanliness of facilities
8.9 Inspection
8.9.1 General
8.9.2 Critical characteristics
36 8.9.3 Self-inspection
8.9.4 Mandatory inspection points (MIPs)
8.9.5 MIPs agreement
8.9.6 MIPs selection
8.9.7 MIPs invitation
37 8.9.8 Inspection and tests status identification
8.10 Specific requirements for assembly and integration
8.10.1 Control of temporary installations and removals
8.10.2 Logbooks
8.11 Manufacturing, assembly and integration records
9 Testing
9.1 General
9.2 Test facilities
38 9.3 Test equipment
9.3.1 General
9.3.2 Verification of test equipment
9.4 Test documentation
9.4.1 Test procedures
9.4.2 Test reports
39 9.5 Test performance monitoring
9.5.1 General
9.5.2 Test witnessing
9.5.3 Test of critical characteristics
9.5.4 Self-certification for test activities
9.5.5 Testing activities subject to QA certification
9.5.6 Testing of hazardous operations
9.5.7 QA authority
9.6 Test reviews
9.6.1 General
9.6.2 QA function representation
40 10 QA requirements for acceptance and delivery
10.1 General
10.1.1 Acceptance process
10.1.2 Preparation of items for delivery
10.2 End item data package
10.2.1 General
10.2.2 Basis for formal acceptance
10.2.3 EIDP objectives
10.2.4 EIDP content
10.3 Delivery review board (DRB)
10.3.1 General
10.3.2 DRB functions
10.3.3 DRB composition
41 10.3.4 Customer participation
10.3.5 DRB responsibilities
10.3.6 Delivery authorization
10.4 Preparation for delivery
10.4.1 Packaging
10.4.2 Marking and labelling
10.5 Delivery
10.5.1 Shipping control
42 10.5.2 Transportation
11 Operations
11.1 General
11.2 Basic quality concepts for operations
11.2.1 Mission quality
11.2.2 Quality of mission products and services
43 11.3 Validation of the system
11.4 QA requirements
11.4.1 QA plan for operations
11.4.2 Operations planning
11.4.3 Operational demonstration
44 11.4.4 Training and operator certification
11.4.5 Operations anomalies and feedback corrective loop
11.4.6 Alerts
11.4.7 Procedural deviations
45 11.4.8 General requirements
46 Annex€A (informative) Ground support equipment (GSE)
49 Annex€B (informative) Logbook€— Document requirements definition
53 Annex€C (informative) End item data package€— Document requirements definition
58 Annex€D (informative) Certificate of conformity€— Document requirements definition
61 Bibliography

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BSI 22/30461479 DC
$13.70