115
โI consider this decision to be problematic and recommend that EU Member States do not repeat the process in the same way. A few weeks of thorough examination by the European Medicines Agency (EMA) is better than a hasty emergency marketing authorisation of a vaccine,โ said Peter Liese, an EU lawmaker who is a member of German Chancellor Angela Merkelโs party.
Britain on Wednesday became the first country in the world to approve the Pfizer-BioNTech COVID-19 vaccine for use and said that it will be rolled out from early next week.
However emergency approval of the experimental COVID-19 vaccine is โproblematicโ as it was done too hastily, a prominent European Union lawmaker said on Wednesday.
โI consider this decision to be problematic and recommend that EU Member States do not repeat the process in the same way. A few weeks of thorough examination by the European Medicines Agency (EMA) is better than a hasty emergency marketing authorisation of a vaccine,โ said Peter Liese, an EU lawmaker who is a member of German Chancellor Angela Merkelโs party.
A vaccine is seen as the best chance for the world to get back to some semblance of normality amid a global pandemic which has killed nearly 1.5 million people and upended the global economy.
โThe government has today accepted the recommendation from the independent Medicines and Healthcare products Regulatory Agency (MHRA) to approve Pfizer-BioNTechโs COVID-19 vaccine for use,โ the government said.
โThe vaccine will be made available across the UK from next week.โ
Britainโs vaccine committee will decide which priority groups will get the jab first such as care home residents, health and care staff, the elderly and people who are clinically extremely vulnerable.
Both Pfizer-BioNTech and U.S. biotech firm Moderna have reported preliminary findings of more than 90% effectiveness โ an unexpectedly high rate โ in trials of their vaccines, which are both based on new messenger RNA (mRNA) technology.
Pfizer said Britainโs emergency use authorization marks a historic moment in the fight against COVID-19.
โThis authorization is a goal we have been working toward since we first declared that science will win, and we applaud the MHRA for their ability to conduct a careful assessment and take timely action to help protect the people of the U.K.,โ said CEO Albert Bourla.
โAs we anticipate further authorizations and approvals, we are focused on moving with the same level of urgency to safely supply a high-quality vaccine around the world.โ
Health Secretary Matt Hancock said the programme would begin early next week. Hospitals, he said, were already ready to receive it.
โIt is very good news,โ Hancock said.
REUTERS