Fact Check: Moderna began clinical trials of COVID vaccine in 2020, not 2017
Data on mRNA vaccines sent by Moderna to European regulators before the COVID-19 outbreak included early tests of the mRNA ...
EurekAlert!14d
High-quality evidence for the treatment of very rare diseases: IQWiG is involved in the EU project RealiseD
High-quality evidence for the treatment of very rare diseases: IQWiG is involved in the EU project RealiseD Developing clinical trials to provide good evidence for very rare diseases, so that ...
Armed robbery in Revesby12d
UK's First In-Silico Regulatory Science Hub Approved
The University of Manchester is bringing together some of the UK's brightest minds from across academia, industry and ...
pharmaphorum2d
Managing the challenges and embracing the opportunities of EU-wide HTA
While the European Medicines Agency (EMA ... The Regulation on Health Technology Assessment (HTAR), passed in 2021 under the auspices of European Network for Health Technology Assessment (EUnetHTA ...
Medscape12d
EMA Expedites Adolescent Chikungunya Vaccine Recommendation
In its first meeting of 2025, the European Medicines Agency ... EMA’s accelerated assessment program because it is considered to be of major public health interest, the agency said in a press ...
JD Supra14d
Key regulatory changes impacting the healthcare industry in the EU and Germany in 2025
The regulatory frameworks in the life sciences and healthcare sector keep evolving rapidly and dynamically. Several important legislative reforms ...
MediWound Initiates the VALUE Global Phase III Pivotal Trial of EscharEx® for Treatment of Venous Leg Ulcers
Phase III trial to assess the efficacy and safety of EscharEx® for debridement and facilitation of active wound closureInterim analysis planned ...
pharmaphorum2d
NICE says yes to BeiGene's Brukinsa after Scottish nay
The final appraisal document from health technology assessment (HTA ... after Brukinsa was approved by the Medicines and Healthcare products Regulatory Agency (MHRA). That approval also included ...
Time21d
What Leaving the WHO Means for the U.S. and the World
On his first day in office, President Donald Trump signed an executive order withdrawing the U.S. from the World Health Organization ... the FDA and EMA [European Medicines Agency], they wanted ...
Le Lézard1d
Biohaven Announces FDA Acceptance and Priority Review of Troriluzole New Drug Application for the Treatment of Spinocerebellar Ataxia
Spinocerebellar Ataxia (SCA) is a rare, genetic, life-threatening neurodegenerative disease with no available treatment.Troriluzole demonstrated a 50-70% slowing of SCA disease progression on the ...
Taiwan News7d
Europe Pharmacovigilance and Drug Safety Software Market Navigating Change A Comprehensive Guide to Future-Proofing Your Business
Request To Download Free Sample of This Strategic Report @ Highlighted with 33 tables and 60 figures, this 119-page report Europe Pharmacovigilance and Drug Safety Software Market 2021-2031 by ...