Demystify Quality Requirements
Demystify Quality Requirements
With our in-depth training and mentoring we can assist you to effectively navigate the often complex environment of medical device quality management.
SERVICES
SERVICES
Medical Device Quality and Regulatory Assurance Specialist Consulting
ISO 13485 Medical device Quality Management System Implementation, Training and Auditing
Regulatory Compliance Consulting
ISO 13485 is the standard that specifies the requirements for a quality management system (QMS) where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and regulatory requirements.
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