REGISTRATION PROCESS - Applies to QMS ISO 9001, EMS ISO 14001, ISO 13485, EMAS, and FSMS ISO 22000, serves as
guidelines for ISMS (Security of Information ISO/IEC 27001), OSHMS (OHSAS 18001 | ILO-OSH | Loss Prevention...), and HACCP MS. We provide guideline documents upon request to client organizations. In
following the same protocols, we verify against FDA CFR requirements and other legal matters. As follows, this is represents a general overview for the certification - registration process.
Completion of the application - questionnaire  provides the
necessary information to investigate your organization and to proceed with presentation of a quote for your evaluation [and may include specifics or other interest on
abiding to requirements such as reference to ISO 15161, EMAS, Sarbanes-Oxley (Section 404), Graham-Leach-Bliley, ASEAN, HIPAA, Loss Prevention... as a truly USA based certification body FDA | CFR].Quote - Application - After your organization evaluates the quote and
selects BRS by agreeing to the terms of business, we commence the planning activities, which includes your organization accepting the assessment team... and proceed to planning of Phase I...
In alignment with ISO/IEC 17024, the assessment team members are exclusively certified for BRS, and it is the organization's acceptance decision of the assessment team.
 Phase I, in-situ is to review documents and verify readiness & planning for Phase II – BRS evaluates
the readiness of your organization to continue the audit protocol toward certification - registration...
This assessment verifies the adequacy of the management system. BRS combines Phase I and Phase II as a advancement protocol, in abiding to International Standards. 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 Registration Assessment – This is continuation 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 requirements of the standard(s)... [and as
contractually agreed includes other requirements such as Sarbanes-Oxley Controls, EMAS, FDA | CFR...]
Granting a Certificate of Registration occurs after successful completing Phase I and Phase II, and the assessment team recommends the organization to an independent body of reviewers.
Phase III, Surveillance Visits – Every 6, 9 - 12 months a surveillance visits objective is to verify the integrity (maintenance, update and
improve) of your organization's management system.
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