Home » EU clears Pfizer COVID-19 vaccine for first inoculations
CORONA Exclusive World

EU clears Pfizer COVID-19 vaccine for first inoculations

EU clears Pfizer COVID-19 vaccine for first inoculations AMSTERDAM 22 December 2020 -The European Union geared up to launch mass vaccinations against COVID-19 just after Christmas after the shot developed by Pfizer and its German partner BioNTech cleared regulatory hurdles on Monday.

European Union countries including Germany, France, Austria, and Italy have said they plan to start vaccinations from Dec. 27 as Europe tries to catch up with the United States and Britain, where inoculations began earlier this month.

Having secured a green light from the European Medicines Agency (EMA), the European Commission gave final approval on Monday evening to the EU’s first COVID-19 vaccine.

Commission President Ursula von der Leyen said doses would be available for all EU countries, at the same time and on the same conditions.

“Today we add an important chapter to a European success story. We approved the first safe and effective vaccine against COVID-19. More vaccines will come soon,” she said.

Preparations for the vaccine roll-out come as the identification of a highly infectious new strain of the coronavirus in Britain caused chaos across the region, with countries shutting off travel ties with the UK and disrupting trade ahead of the Christmas holiday.

EMA officials said it was highly likely the vaccine would work against the new variant of the coronavirus.

EMA executive director Emer Cooke said it would take a long time to inoculate the 450 million people of the 27 EU countries.

RELATED COVERAGE

Student medics retired doctors, pharmacists and soldiers are being drafted into a European vaccination campaign of unprecedented scale.

A phased-in approach means frontline healthcare workers and elderly residents of care homes are being prioritized, with most national schemes not reaching the general public until the end of the first quarter of 2021 at the earliest.

The EMA clearance, initially granted as conditional marketing approval (CMA), is valid for one year and can be renewed annually. It can be converted into a standard marketing authorization after further data checks. This would be valid for five years but can be renewed for unlimited validity.

The process took longer than the ultra-fast emergency authorization given by Britain, the first western country to endorse a COVID-19 shot.

EUROPE’S DRUG TEST

The roll-out will be a test for Brussels’ ability to unify Europe amid political pressure to speed up the process and tame the pandemic which has killed more than 1.6 million people globally.

The EU has ordered 200 million doses of the Pfizer-BioNTech shot, enough to vaccinate 100 million people, paying 15.50 euros ($18.90) per dose.

It will also buy an extra 100 million with a timetable for delivery still to be negotiated.

EMA officials denied any political interference and defended the speed of the approval process.

“The focus was exclusively on the science, there were too many involved of the member states who would look into the science as to allow any political whitewashing or adaption,” said Harald Enzmann, chair of EMA’s Human Medicines Committee (CHMP).

Anupreet Kaur

About the author

Anupreet Kaur

Anupreet Kaur

She's an explorer and highly passionate about writing, painting and traveling. She is dynamic and a natural leader who believes in excellent communication, fearless journalism to pen down her words with the same approach.

Add Comment

Click here to post a comment

All Time Favorite

Categories