Iso 13485 Certification Services

The medical device standard ISO 13485 is a member of the ISO standards family and a specifies requirements for a quality management system that can be used by an organization for the design and development, production, installation and servicing of medical devices, and the design, development, and provision of related servicesa . Medical companies expect this certification from their vendors and Argos is equipped to meet their requirements.
In the field of medical products, devices, and components, regulatory requirements and customer expectations are demanding. Throughout the world, manufacturers and their suppliers are expected to comply with the highest standards and regulations. ISO 13485-a Medical devices is the standard for organizations engaged in the manufacture of medical devices. Designed for new and current auditors interested in sharpening their auditing skills, participants will acquire the necessary skills to become a leader in preparing and conducting 1st and 2nd party audits to ISO 13485
ISO 13485 is an international standard that specifies requirements for a quality management system that can be used by an organization for the design and development, production, installation, and servicing of medical device.