letters of non-US clients

D

dieter

#1
YOu can get a copy of the letters of the european clients from the following internet page of the VDA in GErmany http://www.vda-qmc.de/intro.htm Click on the Screen IAOB and scroll to the bottom. There you will find the letters from the German, French and Spanish car makers. Hope that helps.

If some body needs information from Europe please feel free to contact me.

Regards,

Dieter

NOTE: Reason for edit: URL 'fixed'.



[This message has been edited by Marc Smith (edited 24 February 2000).]
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
S Non-ISO 9001 Suppliers - Customer approval letters to use Supplier Quality Assurance and other Supplier Issues 20
M Always Date format with letters After Work and Weekend Discussion Topics 17
supadrai Indemnity Letters - What's the Deal? Other Medical Device and Orthopedic Related Topics 5
P Warning Letter 1999 - Where does the FDA make older warning letters available? US Food and Drug Administration (FDA) 4
9 EU Medical Device Manufacturer Warning Letters EU Medical Device Regulations 2
K Where you can read other companys' 483 FDA Warning Letters 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
S How do you sign your letters? Coffee Break and Water Cooler Discussions 15
AnaMariaVR2 FDA Global Clampdown: 8 Warning Letters - Failing to Register Plants US Food and Drug Administration (FDA) 0
P Marking Legibility (7.1.2 of IEC 60601-1): Size of Letters IEC 60601 - Medical Electrical Equipment Safety Standards Series 12
AnaMariaVR2 FDA issued Warning Letters to Beckman Coulter - 2011 US Food and Drug Administration (FDA) 1
Ajit Basrur FDA issues Warning Letters for misleading advertising of Lap-Band US Food and Drug Administration (FDA) 3
AnaMariaVR2 The Top 12 FDA 2011 Warning Letters Report US Food and Drug Administration (FDA) 7
A Accents for Letters - National Languages in Medical Device Software EU Medical Device Regulations 5
AnaMariaVR2 FDA has issued three Warning Letters... US Food and Drug Administration (FDA) 13
AnaMariaVR2 4 API Warning Letters focusing on Laboratory Practices US Food and Drug Administration (FDA) 0
F Breakdown and Analysis of FDA Warning Letters US Food and Drug Administration (FDA) 11
D Definition Prints that have a dimension and immediately after it the letters "N. T. S." Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 15
N News Letters for Employee Awareness ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
M First Article Acceptance FAI Letter and related Letters of Approval Supplier Quality Assurance and other Supplier Issues 10
S ISO 9001 - Documentation Control - Letters / Letter Templates Document Control Systems, Procedures, Forms and Templates 4
ScottK Are Cover Letters really necessary? Career and Occupation Discussions 23
Claes Gefvenberg Letters to the editor, anyone? Coffee Break and Water Cooler Discussions 7
Randy Using the letters I-S-O Coffee Break and Water Cooler Discussions 13
D RESPONSE TO NON-CONFORMITIES IATF 16949 - Automotive Quality Systems Standard 4
B Software as a NON-medical device Medical Information Technology, Medical Software and Health Informatics 9
M Is this situation Non-Conformity??? General Auditing Discussions 8
D AS9100 Rev D - Clause 8.7 Control of Non conforming outputs AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
M Non conformance/complaint and CAPA ISO 13485:2016 - Medical Device Quality Management Systems 6
F Product classification according to the 60601-2-57: Particular requirements [...] of non-laser light sources [...] IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
Q API Spec Q1 9th Ed 4.4.2 Non-conformance Oil and Gas Industry Standards and Regulations 8
T Do I need to add non-product related service providers to my ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 12
J ISO 13485- 8.3.1 Non-conforming material high volume ISO 13485:2016 - Medical Device Quality Management Systems 4
F MSA for non-contact CMM - ISO10360 Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
M Using a Non Certified vendor Supplier Quality Assurance and other Supplier Issues 5
somashekar Justification for Non-applicable clause at Stage 2, in clause 4. ISO 13485:2016 - Medical Device Quality Management Systems 11
Z Swiss Authorized representative & non-medical device regulations Other Medical Device Regulations World-Wide 0
R Lead auditor scenario (Need help) is this non conforming to ISO13485 Manufacturing and Related Processes 2
D Help Me. Non conformitty in External Audit IATF 16949 - Automotive Quality Systems Standard 13
S Electronic Signatures - Non-Conformance - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 34
S Do you follow your QMS for non-device software features? Medical Information Technology, Medical Software and Health Informatics 4
J Can we register non-device clinical decision support software under draft guidance? Other US Medical Device Regulations 5
D IATF 16949 SI 10, External non-accredited lab IATF 16949 - Automotive Quality Systems Standard 4
M Selling non-CE marked devices for evaluation EU Medical Device Regulations 4
T Non API products need to comply to API Q1? Oil and Gas Industry Standards and Regulations 3
L "Shelf-Life" Class I Non-Sterile Products Expiration Date? CE Marking (Conformité Européene) / CB Scheme 3
B Process / Procedure - Radiographic (X-Ray) Non-Film Document Control Systems, Procedures, Forms and Templates 0
N How to find column number for the last non-empty column? Using Minitab Software 0
A Need to calculate tolerance Intervals with a set of non-normal data and 3-Parameter Weibull distribution Using Minitab Software 0
3 Non-conformance Register vs Corrective Action Register ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
G Competent Authority non-EU Manufacturer EU Medical Device Regulations 7

Similar threads

Top Bottom