Senseonics has filed to obtain CE Mark registration for its one-year continuous glucose monitoring (CGM) system, Eversense 365. The CE Mark submission aligns with the EU Medical Device Regulation (MDR ...
African National regulatory agencies (NRAs) under the World Health Organisation’s (WHO) maturity level 3, have signed a ...
New Partnership for Africa’s Development (AUDA-NEPAD) and the Africa Centres for Disease Control and Prevention (Africa CDC) ...
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NAFDAC destroys fake products worth N4.7bn in South-SouthThe National Agency for Food and Drug Administration and Control, NAFDAC, has destroyed confiscated fake and falsified ...
W. Edwards Deming Quality culture is a cornerstone of any industry, particularly the healthcare industry where patient lives ...
The Food and Drug Administration Feb. 5 released an alert notifying patients of a safety concern using diabetes devices such ...
Fractures and breakages of the helix on the Rotarex system has led to 30 serious injuries, four deaths, and 115 interventions ...
The FDA approved 16 psychiatric drugs over the last decade, most of which shared similar mechanisms of action with previously ...
New licensing Guidelines issued by the National Institutes of Health at the end of the Biden Administration could harm ...
The new ACC and AHA criteria for cardiac devices emphasize more risk stratification, reflecting advances in the field in ...
Over the past decade, there has been an immense increase in the popularity of health applications and connected health devices as more and more of consumers’ health information is shared online.
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