New UK Biosimilars Pathway Suffers Setback

MHRA Consultation Review Delayed Due To ‘Intense COVID-19 Activities’

The UK’s implementation of a new national licensing framework for biosimilars has been pushed back from the start of 2021, with the MHRA citing “intense COVID-19 activities” as the cause of an indefinite delay in the consultation process.

Alarm Clock COVID coronavirus
The MHRA’s COVID-19 activities have delayed the new pathway • Source: Shutterstock

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