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The Food and Drug Administration (FDA) has extended the review periods for 2 investigational products: sparsentan and tofersen.
The new Prescription Drug User Fee Act (PDUFA) action date set by the FDA is April 25, 2023 CAMBRIDGE, Mass., Oct. 17, 2022Inc. (Nasdaq: BIIB) today announced that the U.S. Food and Drug Administration
British American Tobacco Plc released Thursday the preliminary results of its latest research study, this time evaluating its oral nicotine product Velo of R.J. Reynolds Tobacco Co.
TCELS, in collaboration with the Asia-Pacific Life Sciences cluster, is organising the Bio Asia Pacific 2022 event, linking researchers and investors in support of medical-health research at the industrial level, as well as improving the quality of life and driving the economy forward.