KEMA Quality Registrar
KEMA Quality Management System
KEMA Quality Registrar: ISO Certification
KEMA Quality Registrar
Quality Management System Free Quote
Services

Certification - How it Works

System certification
Process Audits since 1987

+ ISO 14064
 

Regulatory Services

+ ISO 13485:2003
+ CMDCAS - Health Canada
+ ATEX

Other Services

+ Supplier Audits
+ National Biosolids
Are you ready to be a KEMA customer?
KEMA Quality
Filter Type:

      We know how difficult it can be to select a Registrar. You are in a process of selecting a partner that is going to help you with the most important aspect of your company: Quality! We will work with you to determine if KEMA is a right fit for your organization.

Why KEMA?
Other
 Quality Management - New Certification
 Quality Management - Currently Certified
Section I - Company Information
Company Name
Address
City
State
Zip
Contact Name
Contact Title
Phone and ext.
Email
Section II - Additional Company Information
Is your company part of a larger organization?
 Yes No
If yes, please explain


Please list the facilities you wish to include in your certification:
Site Address
City
State
Zip
Number of Employees
Number of Shifts
Site Address State Zip Employees Shifts
Section III - Quality System Information
Please briefly describe your company's products or services
Is the facility(s) to be certified involved in design?
 Yes  No
SIC Code
IAF Code
Please check the standard(s) you wish to be registered to
 ISO 9001:2008 ISO 14001:2004 AS9100C
 TL-9000 TS16949 ESD 20.20
 ISO/IEC 20000 ISO/IEC 27001
Is your company currently certified?
 Yes No
If yes, which standard(s) -
Who is your Registrar?
When is your next audit?
Is it a Renewal or Surveillance Audit?
Why are you looking to Change your Registrar?
Section IV - Quality System Information
Please describe your company’s Products or Services
Do you presently have a fully documented Quality System?
 Yes  No
If no, please explain
If yes, have you completed a full cycle of Internal Audits?
 Yes  No
If not, please explain
Have you completed a full cycle of Management Reviews?
 Yes  No
If not, please explain
When will your documentation be ready for review?
What is your target date for certification?
Section V - The KEMA Certification Process
After reviewing our certification process, please select from the following option. Bare in mind, that form does not commit you to these selections. After consultation with a KEMA team member, you may discover a better, more cost-effective route to certification.

The following options are offered with our certification process. Please select any that you may utilize:
 Process audits during Phase I.
(Audit days are subtracted from the Phase II audit). Additional audit days are not added to the registration.
 Pre-certification audit analysis.
Designed to prepare you for the real audit, these audit results do not count toward or against your actual certification.

Please select only one option below:
Phase 1, Phase 2 and Two Surveillance Audits.
 Three (3) audits

We request two (2) audits over the 3 year contract period; one audit every 12 months.

 Five (5) audits
Five (5) audits over the three (3) year contract period; one (1) audit every six (6) months.

Helpful Links

• Suspended or Withdrawn Certificates
 
ISO Consultants :