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In response to a request for information on medical device cybersecurity by the House Energy and Commerce Committee, stakeholders called for additional guidance and funding to help resolve cybersecurity flaws. Read More
The company will pay $11.5 million to resolve allegations that it caused false claims to be submitted to government healthcare programs for procedures involving an unapproved drug-delivery device. Read More
The Association of Indian Medical Device Industry said Indian devicemakers were ready to comply with the new rules and they should be implemented as soon as possible. Read More
Medical product sponsors and researchers should work with electronic health record keepers to help improve clinical trial accuracy and efficiency, the FDA said in a new guidance. Read More