Actualités réglementaires
21 sept. 2026•1 min de lecture
Regulatory Shift Reduces Comparative Clinical Trials in Biosimilar Development
Large-scale comparative clinical efficacy studies are being scaled back, with global regulators emphasizing advanced quality analysis and PK data, according to a KoBIA report.
Actualités réglementaires
2 sept. 2026•1 min de lecture
FDA approves five new products in June, spanning cell therapy to biosimilars
The FDA granted approvals for five products in June—including a cell therapy, rare‑disease drug, antibiotic, imaging contrast agent and a biosimilar—signaling trends in advanced biopharma.
Actualités réglementaires
30 août 2026•1 min de lecture
Korean Biotech Firms Rank Second Globally in FDA Biosimilar Approvals
Korean companies have secured 19 of the 87 FDA‑approved biosimilars through June 2026, placing Korea second worldwide after the United States.
Actualités réglementaires
23 août 2026•1 min de lecture
PMDA Updates Information on Biosimilars
The Pharmaceuticals and Medical Devices Agency (PMDA) has updated its biosimilars information. Details are available on the PMDA website.