
Regulators delivered a mixed week of drug approvals, safety notices and administrative housekeeping, led by a busy run of US Food and Drug Administration decisions in oncology, biosimilars and consumer drug safety.
The Health Sciences Authority and National Medical Products Administration also refreshed a regulatory cooperation pact, while the Taiwan Food and Drug Administration, ANVISA and Central Drugs Standard Control Organization moved on process measures that could affect how medicines are reviewed, labeled or managed.
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