CS2 (Controlled Shipping Level) by GM - CB notified. What about other customers?

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
J CS2 (Controlled Shipping Level II status) and TS 16949 Registration IATF 16949 - Automotive Quality Systems Standard 10
L Can anyone recommend a Controlled Shipping Provider (CS2), GM approved, in CA? Nonconformance and Corrective Action 2
A Level II Containment or CS2 Controlled Shipping Level 2 Nonconformance and Corrective Action 3
C If my location does not deal with GM - Firewall - CS1 & CS2 Question IATF 16949 - Automotive Quality Systems Standard 3
E CS2 status with one of our customers - Request for Registrar Notification Letter IATF 16949 - Automotive Quality Systems Standard 12
K What Is The Difference Between Cs1 And Cs2 Shipping Levels? GM's GP5 (GM1746) IATF 16949 - Automotive Quality Systems Standard 12
J Supplier Controlled Shipping (GM CS1) Condition Manufacturing and Related Processes 3
T Controlled Forms or documented requirements for records? ISO 13485:2016 - Medical Device Quality Management Systems 2
was named killer AS 9100D - Calibration Instructions - Controlled documents? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
B Do IFU designs have to be document controlled under ISO 13485? Document Control Systems, Procedures, Forms and Templates 2
C Certificate of Conformance Form - COC for each customer a controlled document? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
J Controlled information versus defined documents / records ISO 13485:2016 - Medical Device Quality Management Systems 3
D Controlled Environment requirements Miscellaneous Environmental Standards and EMS Related Discussions 1
C Work Instructions; Controlled/Uncontrolled? Document Control Systems, Procedures, Forms and Templates 5
I Dating controlled documents after changes - Revision History Document Control Systems, Procedures, Forms and Templates 13
qualprod Controlled sticker for product identification? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
Q Do Management Review records have to be on a controlled form? ISO 13485:2016 - Medical Device Quality Management Systems 30
S Controlled Document Location Document Control Systems, Procedures, Forms and Templates 3
GreatNate Document Control info - What is required on a controlled form/document for ISO 9001: 2015? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
G Defect codes and process codes need to be controlled AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
M How to calculate benefits? Moving some developed non controlled software/automation systems Service Industry Specific Topics 2
I R&D prototype documents need to be controlled? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
K Work Order Form (Controlled Document)? Document Control Systems, Procedures, Forms and Templates 5
M Training template - controlled document? Document Control Systems, Procedures, Forms and Templates 21
D Controlled Documents & Note Making ISO 13485:2016 - Medical Device Quality Management Systems 4
pammesue Controlled Setup Sheets for a production line Document Control Systems, Procedures, Forms and Templates 2
P Qualification of a Temperature Controlled Unit have to be empty? Qualification and Validation (including 21 CFR Part 11) 5
M ISO 14644 - Cleanrooms and associated controlled environments -Recovery Test Other ISO and International Standards and European Regulations 0
E Do all Controlled Document copies require a Stamp? Document Control Systems, Procedures, Forms and Templates 3
Uriel Alejandro Including "Internal Rules" as Controlled Documents in a QMS Document Control Systems, Procedures, Forms and Templates 7
J Employer Warning Notice a Controlled Document? Document Control Systems, Procedures, Forms and Templates 7
R How to Cross-Reference Controlled Documents Document Control Systems, Procedures, Forms and Templates 3
C Leveraging previous results in IQOQs - Environmentally Controlled Room 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
R FAI (First Article Inspection) on source-controlled parts AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
M Definition of a controlled document --> is a form a controlled document Document Control Systems, Procedures, Forms and Templates 14
P Employment Application Form - Controlled or Not? Document Control Systems, Procedures, Forms and Templates 3
LeonelAguilar352 Specific Question about Printing Controlled Documents. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
T Controlled Forms - Centralized or Decentralized? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
R Digital Storage of ITAR Controlled Documentation Other ISO and International Standards and European Regulations 7
N Do Material MSDS's Need To Be Controlled? Document Control Systems, Procedures, Forms and Templates 3
C Need examples for Controlled Shipping I and II (CSL) IATF 16949 - Automotive Quality Systems Standard 3
S Is a Dynamic Controlled Form acceptable per 21CFR820 Document Control Systems, Procedures, Forms and Templates 3
T Should a supplier self assessment form be a controlled document? Document Control Systems, Procedures, Forms and Templates 9
D Should Customer Drawings be controlled per AS9100 QMS ? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
M Types of Controlled Documentation - Call Lists of Emergency Contacts Quality Manager and Management Related Issues 5
C Use of white-out or obliterating a portion of a controlled drawing or document Document Control Systems, Procedures, Forms and Templates 7
M Should spreadsheets be controlled? If so, how? Records and Data - Quality, Legal and Other Evidence 8
C Control of Records - Differences between Controlled Documents and Controlled Records Records and Data - Quality, Legal and Other Evidence 18
Q Modification in Controlled Documents AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
A Clean Room as a Controlled Environment - Requirements ISO 13485:2016 - Medical Device Quality Management Systems 12

Similar threads

Top Bottom