UK pharma group posts ‘statistically significant’ trial results for treatment combined with Blenrep pulled in 2022 ...
A case report on a woman who fell sick after eating a zucchini has highlighted the importance of getting an accurate medical history and the role of ...
which allows a drug developer to expedite the review process of its product even if it does not fit the agency's requirements ...
The City of Edmonton marked Métis Week on Wednesday by signing a new memorandum with the Otipemisiwak Métis Government of the ...
A key reason positions haven't been filled is that they require travel that ranges from 25% to 75% of the time.
Before you add some cinnamon to your holiday baked goods, you should check to see if your cinnamon has been recalled. The ...
The U.S. Food and Drug Administration's ("FDA") new advisory committee on digital health is set to examine its approach for evaluating and ...
Abbott's Freestyle Libre 2 and 3 are the first CGMs to receive FDA clearance for use during imaging tests like X-rays, CT scans, and MRIs.
A New York federal judge on Tuesday dismissed about 100 lawsuits that claimed Procter & Gamble , Haleon and other companies ...
“Tapos yung drug list na sinasabi ni Duterte ... I will hang myself in front of you. I will summon, I will sign a waiver, all ...
The Chicago-based medical technology company said the MRI device, called Signa Magnus, had received 510(k) clearance by the U.S. Food and Drug Administration. That approval pathway is for devices that ...