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January 31, 2023
These are some of the key legal deal trends to expect from the health care and life sciences industries in 2023.
January 25, 2023
After another insightful conference this year, these are some of the key legal deal trends to expect from the health care and life sciences industries in 2023.
January 7, 2023
Cyber and physical threats against commercial satellites are no longer a hypothetical discussion. Russia has demonstrated intent and capability to attack
December 30, 2022
Sarah Silbiger/Getty Images, FILE(WASHINGTON) -- A congressional investigation into the Food and Drug Administration's review process for an Alzheimer's treatment found that the agency "deviated" from its standard procedures to approve the Aduhelm drug with inconsistent data. Aduhelm is notable for being the first drug in recent years approved to treat the underlying cause of Alzheimer's, a disease with no known cure that is characterized by progressive dementia that aff...
December 30, 2022
The approval of an Alzheimer's treatment may not have followed standard approval procedures, according to an 18-month investigation by the House Oversight and Reform Committee.
December 29, 2022
The Food and Drug Administration's review process for an Alzheimer's treatment found that the agency "deviated" from its standard procedures to approve the Aduhelm drug.
December 21, 2022
Aman Khera and Dr Christine Moore of Worldwide Clinical Trials share how regulatory agencies are supporting psychedelic research.
December 9, 2022
Genentech has voluntarily withdrawn the US indication for Tecentriq (atezolizumab) for previously untreated urothelial carcinoma.
December 7, 2022
Genentech has voluntarily withdrawn the US indication for Tecentriq (atezolizumab) for previously untreated urothelial carcinoma.
December 6, 2022
Genentech has voluntarily withdrawn the US indication for Tecentriq (atezolizumab) for previously untreated urothelial carcinoma.