Apr 6, 2020
COVID-19
The Medicines and Healthcare products Regulatory Agency (MHRA) announced a set of measures taken to address hazards caused by the outbreak of Coronavirus Disease 2019 (COVID-19) caused by the virus “SARS-CoV-2” or the “novel coronavirus.” These...
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Feb 19, 2020
EU MDR/IVDR
In order to assist all parties involved in operations with medical devices to maintain compliance with applicable requirements under the new framework established by the recent UK Medicines and Medical Devices Bill, special Explanatory Notes have been published. In...
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Feb 17, 2020
Europe
The UK government announced a new bill aimed at the improvement of medical device regulations. It has already passed its first reading on February 11, 2020, and the second reading will take place on March 2, 2020. Overview of the New Bill The new Medicines and...
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Feb 6, 2020
Europe
Assistive technologies refers to technology used to provide necessary support to patients with restricted mobilities or injuries, and to assist them in conducting actions they would be unable to perform without assistance. To provide medical device manufacturers in...
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Feb 4, 2020
Europe
The European Medicines Agency (EMA) and the Medicines and Healthcare products Regulatory Agency (MHRA) issued detailed information on Brexit to assist medical device manufacturers in dealing with issues related to changes associated with the transition period. Due to...
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