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EMA Clarifies Fast-Track Mechanisms For COVID-19 Medicines & Vaccines

 
• By Neena Brizmohun

From speeding up PIP agreements to starting rolling reviews, the European Medicines Agency has explained how it is accelerating its regulatory procedures for COVID-19 treatments and vaccines.

Researchers
Researchers are racing to develop vaccines and treatments for COVID-19 • Source: Shutterstock

The European Medicines Agency has issued a detailed explanation of the rapid regulatory procedures it is making available to fast-track the development and approval of treatments and vaccines for COVID-19, and how developers can best use them.

The procedures, which include speeding up agreements for pediatric investigation plans (PIPs), rolling reviews of marketing applications and the EMA’s priority medicines (PRIME) scheme, are discussed in the EMA’s newly published “

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