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India plans to amend drug trial rules to cut application times and boost efficiency.
The Union Health Ministry in India plans to amend the New Drugs and Clinical Trials Rules to simplify procedures and reduce regulatory compliance times.
Key changes include converting the test license system to a notification process, reducing application processing time from 90 to 45 days, and dispensing with licenses for certain Bioavailability/Bioequivalence studies.
These reforms are expected to cut the number of license applications by about 50%, speed up drug development, and improve regulatory efficiency.
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La India planea enmendar las reglas de ensayos de medicamentos para reducir los tiempos de aplicación y aumentar la eficiencia.