
Medicines regulators in several major markets have issued a mix of approvals, safety communications, supply notices, enforcement actions and procedural updates over the past week.
The latest round-up includes the US Food and Drug Administration (FDA) approval of Trutakna, safety updates from the European Medicines Agency (EMA), a UK approval from the Medicines and Healthcare products Regulatory Agency (MHRA), and further official updates from Japan, Canada, Switzerland, Australia, Brazil, France, India and Italy. The table below summarizes official human medicines regulatory updates from the past seven days.
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