International Qulity Management System        Istituto Servizi Europei Technologici
Home | Sitemap
 
  Home Why CE ?   Services Directives FAQ Contact Us  
Other Certifications
ISO 9001:2008 (Click here to learn more)
ISO 14001:2004 (Click here to learn more)
HACCP/ISO 22000 (Click here to learn more)
ISO 27001 (Click here to learn more)
ISO 20000 (Click here to learn more)
ISO 13485(0Medical Devices) (Click here to learn more)
SA 8000 (Social Accountability Standard) (Click here to learn more)
ISO 9004:2000 (Click here to learn more)
ISO 10002:2004 (Click here to learn more)
ISO 10006:2003 (Click here to learn more)
ISO 10007:2003 (Click here to learn more)
ISO 10015:1999 (Click here to learn more)
ISO 9001, 14001 & 18001 (Click here to learn more)
ISO/IEC 19770-1:2006 (Click here to learn more)
Kaizen (Click here to learn more)
Six Sigma (Click here to learn more)
Lean manufacturing (Click here to learn more)

Is IQMS a Notified body?

No, we are not a notified body. The main reason for this is that when Notified Bodies test products they are not permitted to provide any design assistance relating to the product. By not being a Notified Body, IQMS can give its clients a much more comprehensive service in this regard. It cannot, however, perform the role of a Notified Body and so sub-contracts any such work as required. We have tie-up with different notified bodies.

CE marking in relation to ISO

If you are ISO 9001 certified, then the Standard REQUIRES you to demonstrate conformance of product conformity (national & international).


The inputs includes :-
a) Functional and performance requirements.
b) Applicable statutory and regulatory requirements.
c) Where applicable, information derived from previous similar designs, and
d) Other requirements essential for design and development.

Send Enquiry
*Name :
*Email :
*Contact no :
*Services :
   
Code :