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UK Unveils Go-It-Alone Drug Approval System

Accelerated Reviews Part Of MHRA's Post-Brexit Plans

Executive Summary

Special approval procedures for new drugs and biosimilars, more use of real-world data, a streamlined drug safety monitoring system, and a ‘patient-first culture.’ The MHRA has plenty of ideas in store for its post-Brexit life as a fully independent regulator from January next year.

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