EMA is ready to support the implementation of the new regulation on health technology ... to new medicines. In the European Union (EU), a centrally authorised medicine is accessible to patients when ...

Data on mRNA vaccines sent by Moderna to European regulators before the COVID-19 outbreak included early tests of the mRNA ...

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 ...

The University of Manchester is bringing together some of the UK's brightest minds from across academia, industry and ...

The regulatory frameworks in the life sciences and healthcare sector keep evolving rapidly and dynamically. Several important legislative reforms ...

Improved analytical techniques mean tiny amounts of endocrine disrupting compounds or PFAS can be found in many places. But ...

Pharma: Launch of Shortages Monitoring Platform, several Changes re Clinical Trial Management in EU Countries; Devices: Resolution on the need ...

S.A., a global leader in AI-driven bone microarchitecture imaging solutions, proudly announces 510(k) clearance from FDA and MDR certification in EU for the latest version of its flagship Trabecular ...

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 ...

According to a comprehensive market report authored by DeciBio Consulting LLC, "Single-Cell Analysis (SCA): Market Size, Segmentation, Growth, Competition, and Trends (2024-2029)," the global ...

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 ...