Australia To Use Japanese Reports For Faster Drug Approvals
A total of seven overseas jurisdictions are now covered by the Therapeutic Goods Administration’s process for speeding up drug approvals by using assessment reports from comparable drug regulators.
You may also be interested in...
This is an update of recommendations from the European Medicines Agency's Committee for Medicinal Products for Human Use on the authorization of new medicines in the European Union, and updates on EU marketing authorization changes recommended by the CHMP.
New medicines under evaluation at the European Medicines Agency.
The European Medicine Agency has recommended extending the therapeutic indication of a raft of drugs that are already authorized in the EU.