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Lack of progress on medical device reform legislation has spurred some EU countries to use last year’s joint immediate action plan to improve device oversight. Read More
By 2020, the U.S. FDA will update criteria on antibiotic susceptibility testing devices use to guide appropriate antibacterial drug treatment, under an action plan released by the White House on March 27. Read More
The number of medical devices recalled in the U.S. during the final quarter of 2014 increased over the previous quarter despite an overall drop in the number of recall actions, a report from Stericycle Expert Solutions shows. Read More
Devicemakers have until June 30 to register their products in Malaysia and regulators there are already anticipating a backlog of applications. Read More
Countries looking to develop a medical device regulatory regime should take a total lifecycle approach starting with listing products and implementing premarket controls, the Asian Harmonization Working Party says. Read More