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About ISO 13485:2016 Contract Services. When development and implementation of your ISO 13485:2016 compliant Quality Management System is a priority, and you find yourself short on resources and time, other daily responsibilities sometimes go unattended. In today’s very competitive marketplace, many companies are looking for ways to cut cost.
Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external ...Category: p
The ISO 13485 standard is an effective solution to meet the comprehensive requirements for a QMS. Adopting ISO 13485 provides a practical foundation for manufacturers to address the Medical Device Directives, regulations and responsibilities as well as demonstrating a commitment to the safety and quality of medical devices.
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