A panel of experts at RAPS Euro Convergence 2026 discussed how artificial intelligence (AI) is being applied throughout the ...
The European Parliament and Council have reached a provisional agreement on the Critical Medicines Act (CMA), moving ...
The top observations identified in Form 483 reports from inspections conducted under the recently implemented Quality Management System Regulation (QMSR) include risk management, outsourcing and ...
Malaysia’s National Pharmaceutical Regulatory Agency (NPRA) has begun piloting a fast-track registration pathway for products ...
The International Medical Device Regulators Forum (IMDRF) has released a guidance for manufacturers on how to choose, ...
A panel of European regulators answered questions during a town panel discussion at RAPS Euro Convergence 2026 on the ...
Industry representatives, patients, and regulators shared their perspectives on the reforms to the EU pharmaceutical ...
The US Food and Drug Administration (FDA) is asking for input on repurposing older drugs for new therapeutic uses to address unmet medical needs across a wide range of therapeutic areas. FDA said that ...