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Registration and Assessment Fees

Keeping pace outside the mainstream of fees, our fee structure for ISO 9001, ISO 13485, Regulatory Verifications, ISO 22000, ISO 14001 and EMAS, OSHMS, ISO 45001...ISMS ISO/IEC 27001, HACCP MS, QMS Healthcare and SR&A are globally competitive, and are based to the world region wherein we operate - our accreditation agreement does respects competitive pricing fees to each world's region as we are not forced to maintain a one-price one world policy.

Download table of fees per region in MS Word. For inspection (benchmarking ISO/IEC 17020) and product marking in accordance to regional obligations and regulations, contact the BRS local office.

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, as ISO/IEC 17021, ISO/IEC 27006 and ISO/TS 22003 compliant:

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, ISMS ISO/IEC 27001, and SR&A. 

    Pre-Assessment (optional and not necessary) expectations are that no certification - registration body may carry more than three (3) assessment per year to the same organization as this may constitute advising and consulting.
    This said, pre assessment
    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 certification - 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 sustain, update, and improve the management system on the basis of the organization's objectives.

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 updates and improvements of the organization's performance through the application of the management system.

Notes:

    Under accreditation, 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 International 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

    Accredited Certificates of Registration are typically valid for a minimum period of three (3+) years, we can also arrange extended certification. 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 the International Accreditation Platform requirements of ISO/IEC 17021, ethics and integrity.
    • BRS (see "Sapphire - blue" value) commits not to extend unjustifiable or arbitrary billing days.

    For specific information request our questionnaire and Application) Form, with no obligation, contact us at globalnet at brsltd dot org

     

     

     

 

Copyrights BRS  2017
Last Modified 10 Jun, 2017