The global fight against coronavirus just got stronger as the World Health Organization (WHO) has granted emergency approval for the Covid vaccine made by the Chinese state-owned company Sinopharm.
The WHO on Friday said it had validated the "safety, efficacy and quality" of the Sinopharm jab developed by the Beijing Institute of Biological Products. It further added that this addition has "the potential to rapidly accelerate Covid-19 vaccine access for countries seeking to protect health workers and populations at risk".
Sinopharm is the first vaccine to be developed by a non-Western country to get the green light from WHO. It joins other WHO-approved vaccines including the ones made by Pfizer, AstraZeneca, Johnson & Johnson, and Moderna.
The organization said that the vaccine's efficacy for symptomatic and hospitalized cases of Covid-19 was estimated to be 79%. BioNTech/Pfizer and Moderna have an efficacy rate of around 90% or higher, while the AstraZeneca jab is thought to be around 76%.
One of the main advantages of Sinopharm is that it can be stored in a standard refrigerator at 2-8 degrees Celsius, like the AstraZeneca vaccine.
Pharmacist, Minhal Master (R) administers a dose of the AstraZeneca/Oxford Covid-19 vaccine at a temporary vaccination centre, staffed by pharmacists and pharmacist assistants, at the Al-Abbas Islamic Centre in Birmingham (Photo by OLI SCARFF/AFP via Getty Images)
Prior to the approval, an estimated 65 million doses of Sinopharm have already been administered in China and elsewhere as individual health regulators in various countries, including some in Africa, Latin America, and Asia, have approved the Chinese jabs for emergency use. The vaccine is administered in two doses to those aged 18 and over.
WHO’s approval is significant as it indicates that a vaccine is safe and effective. It also means that the vaccine can be used in the global Covax program, which was set up last year to try to ensure fair access to vaccines among rich and poor nations.
The scheme is reportedly struggling with supply problems and this decision of addition of Sinopharm is expected to boost the program.
Another China vaccine developed by Sinovac, along with Russia's Sputnik, is also under assessment by WHO.
Starmer says the grooming gang inquiry will not be “watered down”
The prime minister confirmed Dame Louise Casey will work with the inquiry
Four survivors have quit the panel, raising concerns over its remit
The inquiry is still finalising its terms and chair
PRIME MINISTER Keir Starmer has said the national grooming gang inquiry will not be “watered down” and will examine racial and religious motives, after a fourth survivor quit the panel.
He was questioned at Prime Minister’s Questions by Conservative leader Kemi Badenoch, who said survivors feared the inquiry was being diluted and their voices silenced.
Quoting survivors, Badenoch said they believed it would “downplay the racial and religious motivations behind their abuse” and asked: “Aren’t the victims right when they call it a cover-up?”
Starmer said survivors had been ignored for many years and that “injustice will have no place to hide.”
He confirmed Dame Louise Casey, whose report recommended a statutory inquiry, would now be working with it. He invited those who had quit to rejoin, adding: “We owe it to them to answer their concerns.”
Jess, not her real name, became the fourth survivor to step down, joining Fiona Goddard, Ellie Reynolds and Elizabeth. Her lawyer Amy Clowrey confirmed her resignation.
Another survivor, Samantha Walker-Roberts, told the BBC she would stay on the panel and wanted the inquiry’s remit widened beyond grooming.
The inquiry, announced in June, is still finalising its terms and chair.
One potential chair, Annie Hudson, withdrew earlier this week over conflict of interest concerns linked to her social work background, while another nominee, former police chief and child abuse expert Jim Gamble, met survivors on Tuesday.
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