The Japanese Yen (JPY) is one of the world’s most traded currencies. Its value is broadly determined by the performance of the Japanese economy, but more specifically by the Bank of Japan’s policy, ...
Experts at the 2025 Clinical Trial Supply Europe will explore supply chain challenges and the impact of AI on trials.
Valneva’s chikungunya vaccine Ixchiq has been greenlit by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) ...
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MyChesCo on MSNOcugen’s OCU400 Receives ATMP Classification from European Commission, Advancing Retinitis Pigmentosa TreatmentOcugen, Inc. (NASDAQ: OCGN) has reached a significant milestone in the development of its gene-agnostic therapy, OCU400, as the European Commission has delivered a positive opinion designating it ...
Berlin: Bayer has announced the submission of a marketing authorization application to the European Medicines Agency (EMA), ...
Telethon Foundation is seeking approval for a gene therapy to treat the rare disease Wiskott-Aldrich syndrome.
President Trump agreed to a 30-day pause in return for concessions on border and crime enforcement with the two neighboring ...
Bayer seeks European marketing approval for use of finerenone in adult patients with HF with a left ventricular ejection fraction (LVEF) of =40%: Berlin Tuesday, February 4, 2025, ...
The two products, both manufactured by Amgen, are aflibercept biosimilars Pavblu and Skojoy. Both biosimilars are indicated ...
Ocugen (OCGN) said it has received a positive opinion from EU regulators for Advanced Therapy Medicinal Product ...
Sarfaraz K. Niazi, PhD, argues that regulatory agencies should eliminate redundant clinical efficacy testing for biosimilars, ...
Imfinzi has been recommended for approval in the European Union, EU, as monotherapy for the treatment of adults with ...
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