SUBSCRIBE NOW

SIGHT

Be informed. Be challenged. Be inspired.

WHO emergency COVID-19 vaccine listing aims to lift access in poor countries

Zurich, Switzerland
Reuters

The World Health Organization on Thursday listed Pfizer and BioNTech’s COVID-19 vaccine for emergency use, in a move seeking to speed access in the developing world. 

The United Nations health agency said it will work with regional partners to tell national health authorities about the two-dose shot and its anticipated benefits. 

Coronavirus vaccines BioNTech and Pfizer

Syringes are seen in front of displayed BioNTech and Pfizer logos in this illustration taken on 10th November. PICTURE: Reuters/Dado Ruvic/File photo

The WHO established its emergency use listing process to help poorer countries without their own regulatory resources quickly approve medicines new diseases like COVID-19, which otherwise could lead to delays. 

The WHO’s review found Pfizer/BioNTech’s vaccine met the “must-have” criteria for safety and efficacy benefits outweigh its risks.

“This is a very positive step towards ensuring global access to COVID-19 vaccines,” said Mariangela Simao, the WHO’s access to medicines program leader. 

“But I want to emphasise the need for an even greater global effort to achieve enough vaccine supply to meet the needs of priority populations everywhere.”

The UN health agency, with the GAVI Vaccine Alliance and the Coalition for Epidemic Preparedness Innovations (CEPI), are spearheading a global effort called COVAX to secure and distribute vaccines to poorer countries, to ensure shots do not go only to wealthy nations. 

The WHO-backed COVAX alliance has agreements for nearly two billion doses, with first deliveries due in early 2021. The alliance has been in talks with Pfizer and BioNTech to secure vaccine.

Even so, the Pfizer/BioNTech vaccine’s challenging storage and delivery requirements, including keeping it at minus 70 degrees Celsius, have made deliveries challenging in western countries, and may pose bigger hurdles for developing nations without adequate infrastructure.

The vaccine has gotten regulatory backing from the United Kingdom, the European Medicines Agency, US Food and Drug Administration, Health Canada, Bahrain, Israel, Kuwait, Mexico, Oman, Qatar, Saudi Arabia and Singapore. 

Pfizer and BioNTech’s messenger RNA vaccine was found to be 95 per cent effective after two doses 21 days apart.

Donate



sight plus logo

Sight+ is a new benefits program we’ve launched to reward people who have supported us with annual donations of $26 or more. To find out more about Sight+ and how you can support the work of Sight, head to our Sight+ page.

Musings

TAKE PART IN THE SIGHT READER SURVEY!

We’re interested to find out more about you, our readers, as we improve and expand our coverage and so we’re asking all of our readers to take this survey (it’ll only take a couple of minutes).

To take part in the survey, simply follow this link…

Leave a Reply

Your email address will not be published. Required fields are marked *

For security, use of Google's reCAPTCHA service is required which is subject to the Google Privacy Policy and Terms of Use.