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
Quote Request Form
KEMA Registered Quality, Inc.
Filter Type:
As you are carefully considering various quality registrars, allow KEMA to provide you with a quote for our services. For immediate assistance, contact the KEMA team now.
How did you find KEMA?
Other
 Quality Management - New Certification
 Quality Management - Currently Certified
Section I - Company Information
Date
Company Name
Address
City
State
Zip
Contact Name
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 Name
State
Zip
Number of Employees
Number of Shifts
Site Name State Zip Employees Shifts
Section III - ENVIRONMENTAL MANAGEMENT SYSTEM AND OCCUPATIONAL HEALTH AND SAFETY MANAGEMENT SYSTEM INFORMATION
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 AS9100B
 TL-9000 TS16949 ESD 20.20
 ISO/IEC 20000 ISO/IEC 27001
Is your company currently certified?
 Yes No
If yes, which standard(s) -
By whom?
When is your next audit?
Is it a Renewal or Surveillance Audit?

If you are only seeking medical certification please complete our Medical Request for Quote form.
Section IV - Environmental Management System Information
Please describe your company’s Products or Services
What is your Standard Industrial Code (SIC)
Have you used a consultant to assist you with the development and/or implementation of your management system?
 Yes  No
If yes, please provide name of consulting company or individual:
Please list any outsourced processes that will be included in the scope of certification:
Do you presently have a fully documented EMS or OH&SMS?
 Yes  No
If no, please explain.
If yes, is it implemented?
Do you have an integrated EMS and Quality Management System (QMS)?
 100% Integrated 75% Integrated 50% Integrated
 25% Integrated No Integration
Are your systems/procedures for training, corrective action, audits, management review, and document control the same for EMS and QMS?
 Yes  No
Please explain
Are your systems/procedures for training, corrective action, audits, management review, and document control the same for OH&SMS and EMS?
 Yes  No
Please explain
Have the environmental aspects, impacts and the associated objectives and targets been fully identified and documented?
 Yes  No
If Yes, list those aspects identified as significant:
If not, please explain
Has there been a site-wide hazards identification and risk assessment been performed?
 Yes  No
If Yes, list the significant or major hazards and risks:
What environmentally related permits are in effect at the site(s) that is (are) being considered for ISO 14001 registration?
What OH&S related permits are in effect at the site(s) that is (are) being considered for OHSAS 18001 registration?
Which of the following special environmental and/or OH&SMS considerations or circumstances are found on or apply to the sites you want included in the scope of your registration
 Underground waterways or lakes / rivers Abandoned buildings/equipment
 Wildlife Site has a hazardous material or Waste storage
 Contact with radiological emitting source Hearing protection is required on a regular basis
 Waste/Water Treatment Facility Bulk Storage
 History of Environmental Excursions Ongoing Remediation/Monitoring
 Recycle program or practice for the product life Employee use of or in contact with potential toxic
For any of the above items checked off, please provide details:
Have you completed a full cycle of Internal Audits?
 Yes  No
Have you completed a full cycle of Management Reviews?
 Yes  No
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:
 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
 
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