Search Results for CAMD

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MDR, IVDR: Competent Authorities Lay Out Road Map By Zachary Brennan - Published 13 November 2017

The Competent Authorities for Medical Devices (CAMD) Executive Group’s EU medical device regulation and in vitro diagnostic regulation (MDR/IVDR) implementation task force has released a road map outlining key challenges and steps for various technical work streams.

Categories: News, Europe, EC, In vitro diagnostics, Medical Devices, Regulatory intelligence, Regulatory strategy


Cash-Strapped MHRA Looks to Stay Flexible By Zachary Brennan - Published 27 April 2016

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) on Tuesday released its business plan for 2016-17, warning of serious financial troubles, particularly as funding for the regulation of medical devices has declined over the past decade and as it's losing revenue from industry because of changes at the EU level.

Categories: News, Europe, EC, EMA, IMDRF, MHRA, NICE, WHO, Biologics and biotechnology, Crisis management, Drugs, Government affairs, Medical Devices, Postmarket surveillance, Regulatory intelligence, Regulatory strategy

Tags: MHRA funding, Brexit, CAMD, ICMRA, IMDRF