Apr 6, 2022
Asia
The new article describes in detail the general principles to be followed concerning the clinical evaluation of medical devices. Table of Contents The Health Sciences Authority (HSA), Singapore’s regulatory agency in the sphere of healthcare...
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Mar 31, 2022
Asia
The article provides a brief overview of the existing regulatory framework for the clinical evaluation of medical devices. Table of Contents The Health Sciences Authority (HSA), Singapore’s regulatory agency in the sphere of medical devices, has...
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May 26, 2021
EU MDR/IVDR
Today marks a landmark event for medical device manufacturers around the globe: the date of full implementation of the EU’s MDR. Starting today all new medical device registrations that fall within the scope of the European Medical Device Regulation (MDR) must be...
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