ISO9001 & IATF16949 Quality department related Documents

ISO9001 & IATF16949 QMS COURSE Master List Of Documents

Department Related All Format in Excel sheet
Category /Name: Master List of Procedures
1 SOP/01 Process for Control of Documents & Record
2 SOP/02 Process for Product & Process Audit
3 SOP/03 Process for Strategic Business Planning
4 SOP/04 Process for Customer Satisfaction
5 SOP/05 Process for HR & Training
6 SOP/06 Process for Manpower Recruitment
7 SOP/07 Process for Handling Abnormality
8 SOP/08 Process for Internal Audit
9 SOP/09 Process for Management Review Meeting
10 SOP/10 Process for Management Review Meeting
11 SOP/11 Process for Control of Monitoring & Measuring Devices
12 SOP/12 Process for NC Customer Complaints
13 SOP/13 Process for Corrective & Preventive Action
14 SOP/14 Process for Marketing
15 SOP/15 Process for Control of NC Products
16 SOP/16 Process for Control of Engineering Specification
17 SOP/17 Process for Inspection & Testing
18 SOP/18 Process for SPC
19 SOP/19 Process for Advanced Product Quality Planning (APQP)
20 SOP/20 Process for Production Part Approval Process (PPAP)
21 SOP/21 Process for Process Failure Mode & Effect Analysis (PFMEA)
22 SOP/22 Process for Initial Product
23 SOP/23 Process for Initial Production Control
24 SOP/24 Process for Production Planning & Service Provision Control
25 SOP/25 Process for Maintenance
26 SOP/26 Process for New Supplier Selection
27 SOP/27 Process for Purchase
28 SOP/28 Process for Tool Management
29 SOP/29 Process for Measurement System analysis (MSA)
30 SOP/30 Process for Material Handling, Storage, Packaging & Delivery
31 SOP/31 Process for Product Identification & Tracebility
32 SOP/32 Process for Rework
33 SOP/33 Process for Error Proofing
34 SOP/34 Process for Continual Improvements
35 SOP/35 Process for Product Safety
36 SOP/36 Process for Temporary Change
37 SOP/37 Process for Escalation
38 SOP/38 Process for Customer Property
39 SOP/39 Process For Control Plan
Document Category /Name: Master List of SYS-Record
1 FR/SYS/01 Master List Of Documents
2 FR/SYS/02 Communication Matrix
3 FR/SYS/03 Resource Planning
4 FR/SYS/04 Management Review meeting
5 FR/SYS/05 Ammendent Realease Note
6 FR/SYS/06 Drawing Issue Records
7 FR/SYS/07 Internal Audit Plan
8 FR/SYS/08 Internal Audit Check Sheet
9 FR/SYS/09 Internal Audit Schedule
10 FR/SYS/10 Product Audit Schedule
11 FR/SYS/11 Non-Conformity Report
12 FR/SYS/12 Internal Audit N.C Summary Sheet
13 FR/SYS/13 ECN/DCN
14 FR/SYS/14 ECN RECORD
15 FR/SYS/15 Product & Process Audit Plan
16 FR/SYS/16 Business Plan
17 FR/SYS/17 Product & Process Audit Report
18 FR/SYS/18 COPQ
19 FR/SYS/19 MOM (Minutes of meeting)
20 FR/SYS/20 Document Change Request
21 FR/SYS/21 Daily 4M Change Monitoring Board
22 FR/SYS/22 Continual Improvement Plan,
23 FR/SYS/23 4 M Change Monitoring Sheet
24 FR/SYS/24 List of internal auditors
25 FR/SYS/25 Matrix Parts & Process Vs Machine
26 FR/SYS/26 Man Machine Matrix
27 FR/SYS/27 4 M Change Hold Tag
28 FR/SYS/28 4 M Change Status&M/c Condition
29 FR/SYS/29 Key Performance Indicator
30 FR/SYS/30 5S Audit Plan & Schedule
31 FR/SYS/31 5s Audit Check sheet
32 FR/SYS/32 4 M Change Request Form
33 FR/SYS/33 MRM Agenda
34 FR/SYS/34 Organizational Knowledge
35 FR/SYS/35 Risk Analysis
36 FR/SYS/36 Context of Organization
37 FR/SYS/37 Interested Parties
38 FR/SYS/38 Circular
39 FR/SYS/39 MOM
Document Category /Name: Master List of NPD-Record
1 FR/NPD/01 Process Flow Diagram
2 FR/NPD/02 Control Plan
3 FR/NPD/03 Operation /Process sheet Standard
4 FR/NPD/04 Part Submission Warant
5 FR/NPD/05 Feasibility Study
6 FR/NPD/06 APQP Time Plan
7 FR/NPD/07 PFMEA
8 FR/NPD/08 APQP Sign Off
9 FR/NPD/09 Master List of Dev. Components of Enquiry receipt register
10 FR/NPD/10 Master List of Drawing
11 FR/NPD/11 Drawing Issue Records
12 FR/NPD/12 Tool Developments Plan(Micro Plan)
13 FR/NPD/13 KAIZEN (Improvement project Report)
14 FR/NPD/14 Packing Standard
15 FR/NPD/15 PPAP Index
16 FR/NPD/16 APQP Matrix
17 FR/NPD/17 IP Tag
18 FR/NPD/18 IPC TAG
19 FR/NPD/19 IPC Observation Sheet
20 FR/NPD/20 IPC Termination sheet
21 FR/NPD/21 Lesson Learnt Sheet
22 FR/NPD/22 Drawing Review format
23 FR/NPD/23 Past Defects History
24 FR/NPD/24 PDCA Records
25 FR/NPD/25 Retro Active Records
26 FR/NPD/26 Special Characterstics
27 FR/NPD/27 Suspected Lot
28 FR/NPD/28 TGR & TGW
29 FR/NPD/29 BOM
30 FR/NPD/30 Checking Aids
31 FR/NPD/31 One Point Lesson
32 FR/NPD/32 List Of CFT Team
33 FR/NPD/33 Master List of Control Plan ,FMEA,W.I
34 FR/NPD/34 FMEA & CONTROL REVIEW PLAN
35 FR/NPD/35 Development Responsibility matrix
36 FR/NPD/36 IP/IPP Log Book
37 FR/NPD/37 Defect Matrix
38 FR/NPD/38 Trial History Sheet
39 FR/NPD/39 Announcement of IPC Starting
40 FR/NPD/40 Announcement of IPC Termination
41 FR/NPD/41 Spec.Meeting
42 FR/NPD/42 Diff.Between CP&Pre-Lunch CP

[vikasgautam]

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[vikrampandey]

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[birender]

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[kkm]

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[prachigedam-iz]

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[ragulvinoth]

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[UPENDRASINGH-xceu]

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[deepaksahoo]

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[MaynkaPandey-fw]

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[SuperSvc]

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[bhupendrachourasiya]

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[sureshc]

Sir please continue with filling with every documents