4DMT Announces Corporate Webcast to Review Interim 52-week Results from the Phase 2b Cohort of PRISM in a Broad Wet AMD Population
Initial interim 52-week results from Phase 2b Population Extension cohort of PRISM clinical trial to be presented by Dante Pieramici, M.D., a ...
istockphoto17d
Fda Food stock illustrations
Choose from Fda Food stock illustrations from iStock. Find high-quality royalty-free vector images that you won't find anywhere else. Video Back Videos home Signature collection Essentials collection ...
istockphoto16d
Fda Illustration stock illustrations
Choose from Fda Illustration stock illustrations from iStock. Find high-quality royalty-free vector images that you won't find anywhere else. Video Back Videos home Signature collection Essentials ...
Reuters27d
US judge blocks FDA graphic warning label requirement for cigarettes
Campbell Barker in Tyler, Texas, on Monday sided with, opens new tab R.J. Reynolds and other tobacco companies in finding the FDA went beyond ... ITG Brands and Vector Group's Liggett Group ...
Reuters3d
US FDA approves AbbVie-Pfizer's treatment for intra-abdominal infections
Feb 7 (Reuters) - AbbVie (ABBV.N), opens new tab said on Friday that the U.S. Food and Drug Administration approved its drug for complicated intra-abdominal infections, including those caused by ...
BBC25d
US FDA officially authorises Zyn nicotine pouches for sale
The US Food and Drug Administration (FDA) has authorised Zyn nicotine pouches to be sold to as a tool to quit smoking cigarettes. Thursday's decision allows 10 Zyn flavours, including mint ...
U.S. News & World Report11d
US FDA Identifies Cybersecurity Risks in Certain Patient Monitors
(Reuters) - The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with certain patient monitors from Contec and Epsimed and urged ...
Al Jazeera English25d
What is Red Dye 3 and why has the US FDA banned it in food and drinks?
In November 2024, nearly two dozen Congress members sent a letter to the FDA officials demanding a ban on the dye. But the decision taken by the organisation also comes amid US President-elect ...
AOL12d
US FDA approves Novo Nordisk's Ozempic to cut risk of diabetic kidney disease progression
(Reuters) -The U.S. FDA has approved Novo Nordisk's Ozempic for reducing the risk of kidney failure and disease progression, as well as death due to heart problems in diabetes patients with ...
The Straits Times19d
US FDA approves standalone use of J&J’s ketamine-derived depression treatment
The US Food and Drug Administration (FDA) has expanded the approval for Johnson & Johnson’s nasal spray Spravato to allow its standalone use in patients with depression, the company said on Jan 21.
Yahoo Finance12d
VectorBuilder Powers FDA IND Approval of World’s First Umbilical Cord Blood-Derived Allogeneic CAR-T Product
Dr. Bruce Lahn, Chief Scientist at VectorBuilder, commented, "Congratulations to Chengdu Ucello on the FDA IND approval of ... cell line for lentiviral vector manufacturing. This production ...