Pharmaceutical industry news
Fresh coverage across pharma, biotech, medtech, research, approvals, and market-moving developments.
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🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Cellular, Tissue, and Gene Therapies Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments-Biologics License Application (BLA) 125842 From Capricor, Inc. for Deramiocel (Human Allogeneic Cardiosphere-Derived Cells)
The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; Rural Health Care Coordination Program Performance Improvement Measures, OMB No. 0906-0024-Revision
In compliance with the Paperwork Reduction Act of 1995, HRSA submitted an Information Collection Req...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; New Animal Drugs for Minor Use and Minor Species
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has b...
Federal RegisterOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher
Protocol for a phase 3, randomized, double-blind clinical trial evaluating the safety and immunogenicity of the MVA-BN® vaccine against mpox in children aged 4 to less than 24 months in the Democratic Republic of the Congo: Data to guide future paediatric vaccination strategies.
Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher
Phase I dose-escalation study of tenecteplase, a third-generation fibrinolytic agent, combined with neuronavigation-assisted stereotactic minimally invasive puncture, in patients with acute spontaneous deep cerebral haemorrhage.
Europe PMCOriginal source






