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In Vitro Diagnostic Medical Devices

An introductory guide has been made available by the Medicine and Healthcare products Regulatory Agency (MHRA) so manufacturers are aware of requirements under the new EU regulations for medical devices (MDR) and in vitro diagnostic devices (IVDR). more

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The Regulatory Affairs Professionals Society (RAPS) is hosting a dedicated workshop on the new EU regulations for medical devices and in vitro diagnostic devices. more

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