iPhone | iPad
Android
Huawei
Volkswagen said this month it needed to cut costs significantly
KT APPDOWNLOAD
Coronavirus: Europe set to approve Covid-19 vaccine in Christmas week
Berlin/Brussels - Germany, France, Italy and five other European states will coordinate the start of their vaccination campaigns, the countries' health ministers said.
Europeans are set to start getting coronavirus vaccines before the new year after the regional drug regulator accelerated its approval process following the launch of immunisation campaigns in the United States and Britain.
The European Medicines Agency (EMA) said an expert panel would convene on Monday December 21 to evaluate the vaccine made by US company Pfizer and German partner BioNTech . It had previously said the meeting could be as late as December 29.
Also read: New coronavirus strain spreading in UK has key mutations, scientists say
While EMA's mandate is to issue recommendations on new medical treatments, the European Commission has the final say on approval and typically follows EMA's advice.
EMA said its expert meeting was brought forward after the companies had provided more data, as requested, and the EU Commission would fast-track its procedures to rule on approval "within days".
Germany should start giving coronavirus shots 24 to 72 hours after the BioNTech/Pfizer vaccine gets EU approval and could begin as soon as Christmas, Health Minister Jens Spahn said on Tuesday.
EU Commission President Ursula von der Leyen echoed those sentiments by saying on Twitter "(It is) Likely that the first Europeans will be vaccinated before end 2020."
Germany, France, Italy and five other European states will coordinate the start of their vaccination campaigns, the countries' health ministers said in a joint statement on Tuesday.
The countries will promote "the coordination of the launch of the vaccination campaigns" and will rapidly share information on how it is proceeding, said the statement, released by Italy.
The statement was also signed by the health ministers of Germany, France, Belgium, Luxembourg, the Netherlands, Spain and EU neighbour Switzerland.
TOUGH CHRISTMAS
Rising infection rates and tighter lockdown measures in many European nations have added to the pressure on the EMA to act as quickly as possible and cast a shadow over the Christmas celebrations.
The EMA added any approval would come with a safety monitoring plan, manufacturing controls, an investigation plan for use in children and binding obligations by the manufacturers to provide more efficacy and safety data.
Britain was the first to approve the shot for emergency use on December 3, followed by Canada on December 9 and the US Food and Drug Administration (FDA) on Dec. 11.
EMA said in early December it planned to issue its view on the BioNTech/Pfizer vaccine by December 29, and on another candidate developed by Moderna by Jan. 12.
Both US biotech firm Moderna and Pfizer-BioNTech have reported vaccine effectiveness in trials of well above 90 per cent - an unexpectedly high rate. Any side effects have eased quickly and had not been serious, they said.
BioNTech reiterated it was on track deliver 50 million doses globally this year, for 25 million two-dose courses needed for immunisation.
More news from
Many told the war revived traumas of past conflicts with some suffering panic attacks after hearing Israeli sonic booms or other loud bangs
Dubai’s real estate market continues to be a global hotspot
Revised dates will be given to applicants who have appointments for September 21, said the Indian Embassy in Abu Dhabi
SmartDeFi and FEG launch innovative platform in emirate
Authorities said that their interior ministry and state security services had opened an investigation into a company's possible ties
The new residential development consists of 180 units
The singer-songwriter, all set to perform live on September 20, talks about filtering out the 'noise', his craziest fan experiences, and AI's impact on music