Registration and Assessment Fees

Our fee structure for ISO 9001, ISO 13485, Regulatory Verifications, ISO 22000, ISO 14001, EMAS, OSHMS, ISMS, HACCP MS, and SrA are competitive, and are based to the world region wherein we operate. For BRS registration protocol (see Phase I through III below)... or inquire through our contact us page questionnaire form for BRS to present a quote:

Phase I - Application Fee [varies according to global region]
Review of level I documents whether on-site, which initiates an advancing certification - registration protocol. Phase I includes an on-site visit as agreed with the organization once determining the total assessment days for QMS 9001, QMS MD ISO 13485, FSMS ISO 22000, HACCP MS, EMS ISO 14001 , EMAS, and ISMS ISO/IEC 27001. 

    Pre-Assessment (optional, not necessary) [Considers regional fee]
    This is a preliminary assessment to review your organization's management system implementation and documentation prior to engaging in Phase I and Phase II of the registration assessment protocol

Phase II - Registration Assessment [Considers that our fees are regionally competitive]
Continuation of Phase I through to complete verification and validation of conformance and effectiveness of the management system and leading to achieve and improve on the basis of the organization's objectives and the management system.

Phase III - Surveillance Assessment [Considers regional fee]
After completion of Phase I and II, achieving registration, once every six (6) months to 9 months BRS verifies and revalidates the effectiveness and demonstrable improvements of the management system.

Notes:

The number of assessors and assessment-days to conduct Phase I and II are based on accreditation requirements [ISO/IEC 17021, ISO/TS 22003, ISO/IEC 27006 and appropriate IAF Guidance] considering:

    • Risk, hazards and technical aspects
    • Size of the organization and logistics
    • Scope of products and / or services
    • Number of facilities & location(s)
    • Complexity of the processes
    • Magnitude of the action, as require

    Certificates of Registration are valid for a minimum period of three (3) years. A certificate of registration continuing annex document is issued resulting from each annual surveillance assessments / reassessment.

    • BRS conducts no more than three 3rd Party assessments per year, in abiding with accreditation requirements ISO/IEC 17021, ethics, and integrity.
    • BRS (see "Sapphire - blue" value) commits not to extend billing days.

    For specific information request our questionnaire and Application) Form contact us at globalnet at brsltd dot org

     

     

     

 

 

 

Copyrights BRS  2008
BRS GlobalNet
Last Modified 28 Apr, 2008