Get iso 13485 certification12/6/2023 ![]() ![]() The International Standard ISO 13485 specifies requirements for a quality management system that can be used by an organization involved in one or more stages of the life-cycle of a medical device including design and development, production, storage and distribution, installation, servicing and final decommissioning and disposal of medical devices, and design and development, or provision of associated activities (e.g. ![]() Become certified by ISO 13485 Medical Equipment Bureau Veritas Certification Denmark A/SĪll organizations today face challenges in following the law requirements for medical devices.
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