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Home PEOPLECERT Certifications Management Systems Professionals ISO 13485 Regulatory Requirements for Medical Devices M.S.*
ISO 13485 Regulatory Requirements for Medical Devices M.S.* (Coming Soon)

The purpose of the PEOPLECERT certification is to verify professional skills and competence against the criteria set by ISO 13485 and is relevant to those professionals responsible for their organization’s Quality of Medical Devices.

ISO 13485 identifies the principles for a quality management system where an organization wishes to validate its competence in providing medical devices and related services that consistently meet customer requirements and regulatory requirements.

ISO 13485 - Medical Devices Quality