REGISTRATION PROCESS - Applies to QMS ISO 9001, EMS ISO 14001, ISO 13485, QMS Healthcare, 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 in accordance with FDA CFR. As follows, this is represents a general overview for the accredited certification -
registration process. Completion of the application - questionnaire  provides the
necessary information to proceed with an initial investigation and followed by a quote for your perusal [and may include specifics or other interest on abiding to
regulatory requirements such as compatibility with FDA | CFR and others].Quote - Application - After your organization selects BRS by agreeing to the terms of business and quote, together 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 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 by benchmark internationally acceptable 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 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
[and as contractually agreed may include 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 board of reviewers and the reviewers concur.Phase III, Surveillance Visits – Per agreement, 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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