REGISTRATION PROCESS - Applies to QMS ISO 9001, EMS ISO 14001, EnMS 50001, ISO 13485, QMS Healthcare, SMS 28000, and FSMS ISO 22000, serves as guidelines for ISMS (Security of Information ISO/IEC 27001), OSHMS (BS OHSAS 18001 | ILO-OSH | ISO 45001, Loss Prevention...CFR), and HACCP HARPC MS. We provide guideline documents upon request to client organizations. As follows, this represents a general overview for BRS accredited certification - registration process.

Completion of the application - questionnaire provides the necessary information to proceed with an initial investigation and to follow with a quote for your perusal [and may include specifics or other interest on abiding to regulatory requirements]. BRS assessors are ready to the Annex SL.

Quote - Application - After your organization selects BRS together we commence the planning activities, which includes your organization accepting terms and conditions of mutual respect, the assessment team and proceed to planning of Phase I...

In alignment with ISO/IEC 17024 - accreditation, the assessment team members are exclusive BRS professionals, and it is the organization's acceptance decision of the assessment team.

Phase I, in-situ is to complete initial assessment to verify the readiness of the management system and  planning for Phase II continuing the audit protocol toward certification - registration... This assessment verifies the adequacy of the management system. BRS requires Phase I and Phase II as a advancement protocol under accreditation. From Phase I to Phase II there is a limit time period.

Phase I provides the flexibility to work in team with your organization staff as best suited to your needs.

Phase II, Finalizing the Registration Assessment – This is continuation of the certification protocol from Phase I... continuing in-situ | on-site assessment of your organization's management system; the BRS assessment team evaluates, analyses, and reports the effectiveness of implementation and updates in accordance with the contractual requirements [which contractually agreed may include other requirements such as Sarbanes-Oxley Controls, EMAS, FDA | CFR...]

Granting a Certificate of Registration occurs after successful completion of Phase I and Phase II, and  the assessment team recommends the organization to an independent and competent board of reviewers for concurrence to the recommendation.

Phase III, Surveillance Visits – Per agreement, every 6, 9, 12 months a surveillance assessment is to verify the integrity (maintenance, update and improve) of your organization's system.

To verify certification status, suspension or withdrawal please contact us. We abide to contractual agreements as well as consumer-centric accreditation protocols in the protection of privacy and confidentiality as determined by US laws.