ISO 13485 Certification for Medical Device Manufacturer
Information about QMS 13485 certification requirements and procedures for medical devices (by Charles Wilson)
ISO
13485 Certification
is an effective solution for these expanded requirements for quality management
system (QMS) requirements of Medical Devices. Adoption of ISO 13485 provides a practical
basis for manufacturers to deal with the rules and responsibilities, as well as
demonstrating a commitment to the safety and quality of medical devices.
