The emergency use of (hydroxy)chloroquine, enlisting supercomputer power, relaxing the rules on coordinated supply strategies, and harmonizing COVID-19 reporting terms at global level – these are just some of the many avenues regulators and companies have been taking over the past week or so as the pandemic changes much of what we thought we knew about drug regulation.
There has been much pandemic-related activity in the EU, where the European Medicines Agency says it has had held discussions with developers of around 40 potential treatments and a dozen vaccines against the coronavirus, noting that two vaccines have already entered Phase I clinical trials
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