Accelerated

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ISO 13485

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Accelerated Group is one of the world's leading consulting companies and provides training, consulting certification, automation, internal audits, acquisition audits, supplier audits, FDA Audits and CGMP Audits for worldwide standards.

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Consulting, Training, Certification, Supplier Management, and Auditing Services:

We offer written guaranteed consulting, training, certification, and auditing services for worldwide standards for ISO 13485.

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ISO 13485 Online Training by Standard:

CE Marking (90/385) for Active Implantable Medical Devices- Essential Requirements Only
CE Marking (90/385) for Active Implantable Medical Devices- Implementation and Auditing
CE Marking (93/42 ECC) for medical devices- Essential Requirements only
CE Marking (93/42 ECC) for medical devices- Implementation and Auditing
CE Marking IVD 98-79 EEC Implementation and Auditing
CE Marking IVD 98-79 EEC Implementation and Auditing, Essential Requirements Only
FDA-GMP Good Laboratory Practice for nonclinical (21 CFR part58) Implementation and Auditing.
FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requirements
FDA/CGMP Blood - Implementation & Audit/Auditor
FDA/CGMP Drug (Pharmaceutical) - Implementation and Audit/Auditor (21CFR210-211)
FDA/CGMP Food - Implementation & Audit/Auditor
FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation
FDA/CGMP Medical Devices Introduction & Employee Overview
FMEA, Risk Analysis for Medical Devices
ISO 13485 Executive Management Review meeting ISO 13485
ISO 13485 Internal Auditing/Auditor and Implementation in Chinese
ISO 13485: Internal Auditing /Auditor and Implementation
ISO 13485: Introduction & Awareness for meeting ISO 13485 requirements
ISO 14971 Risk Management Implementation & Auditing/Auditor meeting FDA /ISO13485/CE Marking
ISO 9001:2008: Executive and Management Review for meeting ISO 9001:2008 requirements
Quality Improvement Concepts -continuous improvements-problem solving and customer satisfaction
RISK Management Employee Overview for Medical Device meeting ISO 14971/ISO 13485/FDA/CE MARK
Safety Risk Assessment, Calculation Method, Hazard Identification, and Risk Control for OSHA 18001