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Is Your Medical Device Software Compliant with the New EU Standards?

The IEC 62304 standard specifies life cycle requirements for the development of medical software and software within medical devices. It is a standard that is harmonized between the European Union (EU) and the United States...more

8/31/2017  /  EU , Manufacturers , Medical Devices , Software

New Guidelines for Examination of Computer Related Inventions in India

On July 3, 2017, revised Guidelines for Examination of Computer Related Inventions (CRIs) were released. The full text of the guidelines may be found here. ...more

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