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...
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 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.