A class-action lawsuit alleges that Medtronic shared patient data with third parties.
A class-action lawsuit filed against Medtronic plc alleges that the medtech giant illegally distributed personally identifiable data and protected health information gathered by apps connected to customers’ MiniMed insulin pumps and InPen smart insulin pens to Google LLC and other third parties.
According to the lawsuit, filed by the anonymous plaintiff “A.H.” in US District Court in Central California, the protected health...
Ahead of the 11 June UK spending review and its anticipated funding uplift for healthcare and life sciences, the MHRA announced an expansion of its digital expertise by creating a dedicated hub in Leeds, a renowned center of medtech excellence.
FDA moves forward with implementing previous draft guidance and will consolidate forms, but the agency estimates limited impact in the total reporting burden.
The US FDA's new draft guidance details the responsibilities of new owners of 510(k) clearances, including making timely updates device listings in FURLS and GUDID to maintain accurate information for safety alerts and recalls. Comments on the draft are accepted until 4 August.
