WASHINGTON – Leading American infectious disease scientist Anthony Fauci yesterday walked back his criticism of Britain’s drug regulator after saying it had rushed through its coronavirus vaccine approval.
His comments came a day after Britain became the first country to approve the Pfizer-BioNTech Covid-19 vaccine for general use, prompting some skepticism among the country’s European neighbours and suggestions of politicisation.
Widely respected Fauci, who leads the United States National Institute of Allergy and Infectious Diseases, told the BBC: “I have a great deal of confidence in what the United Kingdom does both scientifically and from a regulator standpoint.”
“Our process is one that takes more time than it takes in the UK. And that’s just the reality,” he said, adding: “I did not mean to imply any sloppiness even though it came out that way.”
Fauci had earlier described Britain’s Medicines and Healthcare products Regulatory Agency (MHRA) as having “ran around the corner of the marathon and joined it in the last mile” and “rushed through that approval”.
He contrasted that with the US Food and Drug Administration (FDA), which he said had been careful to avoid “cutting corners” because it did not want to fuel vaccine skepticism.
“In fact, they were even rather severely criticised by their European Union counterparts who were saying, you know, ‘That was kind of a hot dog play,’” Fauci had said.
Fauci made his original comments ahead of his first meeting with President-elect Joe Biden, which Biden told CNN took place yesterday afternoon as the US enters its worst-ever phase of the pandemic.
June Raine, the head of the MHRA, had previously insisted that “no corners had been cut” in vetting the vaccine.
Deputy chief medical officer for England, Jonathan Van-Tam, also hit back at critics, telling the BBC: “If you're a regulator who’s slightly further behind, what do you say to justify your position that you are further behind? Words such as the ones we've heard perhaps.”
Britain’s MHRA was also praised Wednesday by Moncef Slaoui, a former pharmaceutical executive turned chief advisor of the US government’s Operation Warp Speed programme to develop Covid-19 vaccines and treatments.
He told reporters on a call that the British agency was on a par with the FDA as the world’s best regulator, and described it as being the “scientific engine” of the European Medicines Agency before Britain left the organisation following Brexit.
An advisory panel of the FDA is holding a public meeting on December 11 to evaluate the same vaccine, and approval could follow shortly after.
The EU for its part has insisted the bloc has not fallen behind.
German Health Minister Jens Spahn, addressing a videoconference of his EU colleagues, said Wednesday: “The idea is not to be first, but to have a safe and efficient vaccine.”
“It is a matter of expertise, obviously, authorisation. But as we’ve seen from comments from the UK, it's also a political issue for the European Union,” he added. – AFP, December 4, 2020
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