FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
'Watershed moment': Experts call for hyperbaric chamber regulations after child's death
Industry leaders say the government failed to protect Thomas Cooper, 5, from dying in a hyperbaric chamber fire at the Oxford ...
Medical Dialogues15h
Govt Reconstitutes DTAB, AIOCD Protests Exclusion from Drug Regulatory Body
The Central Government, through a notification issued by the Ministry of Health and Family Welfare has officially ...
In wake of child's death, industry leaders call for regulation of hyperbaric chambers
Industry leaders say government failed to protect Thomas Cooper from dying in a hyperbaric chamber fire at the Oxford Center ...
Med Device Online5d
Key QMS Considerations For Your Medical Device Startup
A quality management system (QMS) can often become bloated and unwieldy. This expert helps you understand key QMS basics and ...
Medical Design & Outsourcing4d
De-risking medical device startups with a systematic approach to innovation
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
Medtronic slips after FDA notice on product recall (update)
Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...
FDA Recalls Nearly 200,000 Cans of Green Beans for Potential Contamination
The U.S. Food and Drug Administration issued a Class II recall notice to take back 8,242 cases (197,808 cans) of Good & ...
Reuters5d
FDA classifies recall of Medtronic embolization devices as 'most serious'
March 18 (Reuters) - The U.S. Food and Drug Administration on ... recalled products and has notified regulatory agencies globally as appropriate. The devices in question are used to treat bulges ...
Alnylam's Amvuttra Secures FDA Approval For Expanded Use For Rare Heart Disease, Stock Jumps
The approval expands the indication for Amvuttra, which now becomes the first and only therapeutic approved by the FDA for ...
IceCure Reports Updated Timeline and Progress with FDA Regarding Marketing Authorization for ProSense® Cryoablation in Early-Stage Breast Cancer
IceCure Medical Ltd. (Nasdaq: ICCM) ("IceCure", "IceCure Medical" or the "Company"), developer of minimally-invasive ...
Alabama lawmakers advance regulations on pharmacy benefit managers
Alabama lawmakers on Thursday advanced proposed regulations on pharmacy benefit managers. Supporters said the bill is needed ...