The CRO Group Inc.
Crogroup.com: Medical device, IVD, and biotechnology consulting in quality, regulatory, safety testing, clinical investigations, reimbursement, export, compliance, approvals, ISO9000, EN46000, ISO13485 certification, CE Marking, 21CFR820, 21CFR812, authorized representative, software-qa, mdr-vigilance, and ipo-venture capital audit preparations
crogroup.com
Title: "The CRO GROUP, Inc., ISO 13485, CMDCAS, QSR and Part 11 experts"
Description: We are a global consulting organization for medical, biotechnology, and in vitro diagnostic device
companies in ISO 13485 and CMDCAS registration preparation, CE Marking, Part 11 and software 510(k)s, and international registrations.
Keywords: iso 13485 cmdcas ivd directive 510k en 60601-1-4 21 cfr 11 21 cfr 812 21 cfr 820 part 11 eu authorized representative fda us agent technical files quality systems safety testing 93-42-eec 98-79-ec
