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Serum applies for EU Covishield nod through AstraZeneca

By Sohini Das
June 30, 2021 12:11 IST
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We have applied for marketing authorisation to the EMA through AstraZeneca. We will not sell the vaccine in the EU, said a company source.

IMAGE: Kindly note that this image has been posted for representational purposes only. Photograph: Dinuka Liyanawatte/Reuters.

Amid concern around visits to Europe by individuals who took the jab of Serum Institute of India (SII), company sources have said SII has applied for marketing authorisation before the European Medicine Agency (EMA) through British drug­maker AstraZeneca, its vaccine partner.

 

So far, 287 million Covishield shots, single and double, have been given in India, and the company has exported close to 70 million doses.

SII Chief Executive Officer Adar Poonawalla said on Monday he had taken it up at the “highest levels”. If European Union (EU) restriction on Covishield continues, at least a few hundred million people would face challenges entering or travelling within the EU member States.

“We have applied for marketing authorisation to the EMA through AstraZeneca. We will not sell the vaccine in the EU. But, since this is a technicality to ensure that those who got Covishield shots gain entry into the EU member countries, we have applied for marketing authorisation,” said a company source, adding that the issue should be resolved within a month or so.

The person added Covishield was recognised by the Medicines and Healthcare Products Regulatory Agency of the UK, and SII has supplied this vaccine to the UK and Canada apart from low- and medium-income countries (LMICs).

SII did not wish to divulge more detail on the matter or whether it had applied through AstraZeneca. ANI quoted an EU official saying, “… as of yesterday, the EMA stated that it had not received a request for approval. It will examine any such request when received...”

Meanwhile, the African Union Commission and the Africa Centres for Disease Control and Prevention have urged the European Commission to consider increasing mandatory access to those vaccines deemed suitable for a global roll-out through the EU-supported COVAX facility.

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Sohini Das in Mumbai
Source: source
 
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