India’s new draft list explains how over 700 medical devices and IVDs will be classified under new rules that will come into force in January 2018.
India’s healthcare products regulator has published a draft list of over 700 medical devices and IVDs clarifying how these products will be classified under new rules governing medtech that are scheduled to kick in next year.
The new Medical Devices Rules, 2017, published by the Central Drugs Standard Control Organisation and...
After multiple warning letters and safety communications, the US FDA has decided to block the import of certain endoscopes from Olympus. In total, the agency’s action pertains to 58 device models manufactured by the Japanese firm used in urinary, respiratory, abdominal and pelvic procedures.
Healthcare product industries await publication of the NHS 10-Year Plan, due out the coming days, which will focus on health generally not just the NHS, UK health secretary Wes Streeting said during a final prelaunch event on 24 June.
From June 30, new European Commission rules will attempt to redress an imbalance in medtech trade between the EU and the People’s Republic of China.
