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EMA
Biotech
More collaborative FDA can accelerate rare disease R&D: report
The National Academies is recommending the FDA and European Medicines Agency implement a “navigation service” to advise on regulatory pathways.
Nick Paul Taylor
Sep 13, 2024 5:00am
PTC deepens layoffs as DMD drug faces loss of EU authorization
Sep 29, 2023 8:51am
CureVac giving up on first COVID mRNA vaccine
Oct 12, 2021 7:40am
Parexel hiring spree continues as it nabs regulator alumni
Jul 27, 2020 8:20am
EMA starts accelerated review of Gilead's remdesivir
May 1, 2020 6:00am
As Brexit nears, Britain's drugs, devices and pricing regulators seek the exit
Aug 22, 2019 9:00am
