Approving distributors as suppliers for automotive company

#1
Does anybody have the experience of approving distributors as suppliers for the automotive company?
How do you assess the QMS of such supplier without assessing the actual manufacturing site?
How do you approve the parts (PPAP)?
How do you confirm the production run? Etc.
Thanks in advance for any reply.
 
Elsmar Forum Sponsor

John Broomfield

Leader
Super Moderator
#2
Start with the needs of your customers and your distributor selection criteria.

Which aspects of service performance are most important to your customers?
 
Thread starter Similar threads Forum Replies Date
C Approving AWS as a supplier (ISO 13485) ISO 13485:2016 - Medical Device Quality Management Systems 4
M Suitable form or questionnaire for approving consultants Document Control Systems, Procedures, Forms and Templates 9
N Understanding, Challenging & Approving Supplier Control Plans FMEA and Control Plans 7
R Question of Approving Documents ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
JoCam Approving a Test House on a Medical Device as a part of a 510k Submission 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
Q Approving Software Suppliers in an AS9100 Company AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
R Approving a New Hand Assembly Line at a Supplier Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
R Approving Suppliers by "Grandfathering" ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
N Role of Quality Function in Approving Work Instructions Document Control Systems, Procedures, Forms and Templates 4
Q AS9100 Clause 8.3 - Control of Nonconforming Product Process for Approving Personnel AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
T Approving Consulting Firms in a Medical Device Company ISO 13485:2016 - Medical Device Quality Management Systems 25
T Approving Suppliers - Approving Marketing Companies Other ISO and International Standards and European Regulations 10
P Originating and Approving Internal Procedures Document Control Systems, Procedures, Forms and Templates 9
L Approving myself as a Supplier - Should we be on our own ASL AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
M Gage R&R for Big Parts - Approving a Variable Gage using only 1 Part Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
G Does AS9100 require approving your Customer as a Supplier? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
J Re-approving documents when the responsible person leaves or changes responsibilities ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
A Qualifying and Approving Equipment for Welding AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
A Process for Approving Personnel Making Decisions - AS9100 Clause 8.3 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
B Approving Suppliers - Consultants AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
J Approving Suppliers under 7.4.1 - Approved Suppliers List - ISO 9001:2000 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
T Approving Suppliers under 7.4.1 - AS9100 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 20
Anerol C Who is Approving your Manufacturing Visual Aids / Process Sheets? Document Control Systems, Procedures, Forms and Templates 6
T Approving documents prior to issue - What guarantees their adequacy? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
C Distributors Agreement Article 14 EU Medical Device Regulations 4
K Critical Material Vendors: Distributors Vs Manufacturers and Supply Agreements ISO 13485:2016 - Medical Device Quality Management Systems 1
A Distributors with stock of expired CE marking EU Medical Device Regulations 2
A MDR Article 16 Certification of Distributors by a Notified Body? EU Medical Device Regulations 8
B ASTM, Steel HEat traceability and mixing at distributors/reprocessors Various Other Specifications, Standards, and related Requirements 0
Ed Panek Does this FDA Requirement Apply to international (not USA) distributors for USA based manufacturing companies? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
C Requirements for distributors under MDR: translation EU Medical Device Regulations 0
M Responsibilities of Importers / Distributors - MDR EU Medical Device Regulations 7
J Marking "Distributed By" to product with distributors' reference-code EU Medical Device Regulations 3
D Approved supplier list - Distributors question ISO 13485:2016 - Medical Device Quality Management Systems 6
T Different Authorized Representative and distributors in Saudi Arabia Other Medical Device Regulations World-Wide 0
T PPAP for distributors? APQP and PPAP 1
C ASL - Buying from unqualified manufacturers through qualified distributors Supplier Quality Assurance and other Supplier Issues 2
S Degree of control of distributors - PMS EU Medical Device Regulations 2
R Qualification of Distributors such as McMaster-Carr and Digikey to Medical Device Companies ISO 13485:2016 - Medical Device Quality Management Systems 3
JoCam Distributors Responsibilities - Medical Device Recalls EU Medical Device Regulations 1
H Supplier Development - Distributors only? The new GM Standards IATF 16949 - Automotive Quality Systems Standard 4
T Oversight of Distributors - Supply chain requirements under the MDR EU Medical Device Regulations 9
Sidney Vianna Informational UTC ASQR Rev.11 has a mistake; certification of distributors to IATF 16949 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
I ISO 9001 and VWAD (Verified-Accredited Wholesale Distributors certification) Coffee Break and Water Cooler Discussions 1
C Do Distributors need to register with competent authorities in the EU? EU Medical Device Regulations 2
JoCam Medical Device Certificates of Free Sale - Distributors EU Medical Device Regulations 9
J Recall Effectiveness - Accessory to Medical Devices shipped through Distributors Customer Complaints 3
D Customer Specific Requirements / Distributors (IATF 16949) Customer and Company Specific Requirements 1
H Local Representative / Distributors - United Arab Emirates Other Medical Device Regulations World-Wide 2
Sidney Vianna IAF Endorsed Accredited 13485 Certification helping Control of Medical Distributors ISO 13485:2016 - Medical Device Quality Management Systems 0

Similar threads

Top Bottom