Medical Device Related Standards

Medical devices standards, national and international. Standards are published by standards writing bodies (such as ISO and IEC internationally, ANSI, CEN, CENELEC, CSA and others nationally) and are generally voluntary. You can use standards to fulfill regulations, depending on the way the regulation uses standards.

ISO 13485:2016 - Medical Device Quality Management Systems

ISO 13485 - Medical Device Quality Management System Requirements for Regulatory Purposes - (ISO 14969 has been replaced by ISO 13485:2016).
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Discussion Threads
2,612
Posts
19,546

ISO 14971 - Medical Device Risk Management

ISO 14971 - Medical Device Risk Management and Hazard Control: Identifying and controlling the risks and the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices.
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317
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2,805
Discussion Threads
317
Posts
2,805

IEC 60601 - Medical Electrical Equipment Safety Standards Series

The IEC 60601 standards series covers safety and performance issues of medical electrical equipment, and also topics such as EMC and alarms. This sub-forum includes collateral (IEC 60601-1-X) and particular (60601-2-x) standards.
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902
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5,536
Discussion Threads
902
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5,536

IEC 62304 - Medical Device Software Life Cycle Processes

IEC 62304 - Requirements for a development life cycle of medical device software, including medical device software risk management.
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209
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1,522
Discussion Threads
209
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1,522

IEC 62366 - Medical Device Usability Engineering

Application of usability (human factors engineering) engineering to medical devices.
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53
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528
Discussion Threads
53
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528

Other Medical Device Related Standards

Medical Device Related Standards not listed in the above sub-forums.
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2,413
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