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2. ISO 14971 - Wikipedia

   en.wikipedia.org/wiki/ISO_14971

   The third edition of ISO 14971 was published in December 2019 and supersedes the second edition of ISO 14971. [ 5 ] Specifically, ISO 14971 is a nine-part standard which first establishes a framework for risk analysis, evaluation, control, and review, and also specifies a procedure for review and monitoring during production and post-production.

3. List of ISO standards 14000–15999 - Wikipedia

   en.wikipedia.org/wiki/List_of_ISO_standards_14000...

   ISO/IEC 15444-8:2007 Secure JPEG 2000; ISO/IEC 15444-9:2005 Interactivity tools, APIs and protocols; ISO/IEC 15444-10:2011 Extensions for three-dimensional data; ISO/IEC 15444-11:2007 Wireless; ISO/IEC 15444-12:2015 Part 12: ISO base media file format [Withdrawn, no replacement] ISO/IEC 15444-13:2008 An entry level JPEG 2000 encoder

4. Risk management - Wikipedia

   en.wikipedia.org/wiki/Risk_management

   The European version of the risk management standard was updated in 2009 and again in 2012 to refer to the Medical Devices Directive (MDD) and Active Implantable Medical Device Directive (AIMDD) revision in 2007, as well as the In Vitro Medical Device Directive (IVDD). The requirements of EN 14971:2012 are nearly identical to ISO 14971:2007.

5. List of ISO standards 24000–25999 - Wikipedia

   en.wikipedia.org/wiki/List_of_ISO_standards_24000...

   ISO/IEC 24824-1:2007 Fast infoset; ISO/IEC 24824-2:2006 Fast Web Services; ISO/IEC 24824-3:2008 Fast infoset security; ISO/TR 24971:2013 Medical devices – Guidance on the application of ISO 14971; ISO 24978:2009 Intelligent transport systems – ITS Safety and emergency messages using any available wireless media – Data registry procedures

6. List of ISO standards - Wikipedia

   en.wikipedia.org/wiki/List_of_ISO_standards

   Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

7. ISO 10993 - Wikipedia

   en.wikipedia.org/wiki/ISO_10993

   The ISO 10993 set entails a series of standards for evaluating the biocompatibility of medical devices to manage biological risk. These documents were preceded by the Tripartite agreement and is a part of the international harmonisation of the safe use evaluation of medical devices . [ 1 ]

8. images.huffingtonpost.com

   images.huffingtonpost.com/2012-08-30-3258_001.pdf

   Created Date: 8/30/2012 4:52:52 PM

9. List of ISO standards 30000–99999 - Wikipedia

   en.wikipedia.org/wiki/List_of_ISO_standards_30000...

   ISO/ASTM 52900:2015 Additive manufacturing – General principles – Terminology; ISO/ASTM 52915:2016 Specification for additive manufacturing file format (AMF) Version 1.2; ISO 53800:2024 Guidelines for the promotion and implementation of gender equality and women’s empowerment; ISO 55000:2014 Asset management – Overview, principles and ...