The UK government persuaded the Oxford team to work with AZ back at the start of the pandemic. AZ were going to go in with Merck (Who bailed out of their program this week) but were persuaded to switch with funding and they developed the current vaccine as one that was essentially developed in the UK.
Part of the deal was UK government investment in AZ covid reasearch. As a country, our scientific expertise in this field - sequencing the virus etc is second to none. Early sign up enabled the UK manufacturing sites scale up to trouble shoot issues early and resolve them. The UK supply of AZ vaccine had pretty much the same difficulties as the Belgium sites have now, except the UK ones are now over them and working at max capacity. The EU sites are now hitting the same scale up issues, and have to go through the same learning curve. Hence the delay to EU AZ vaccine access.
Aside of the fact that the EU have still not approved (until today) the AZ vaccine, they complain about their restricted access to something they have not approved the use of, and then the main player Germany says it should not be used in the most vulnerable over 65's!!
As a company, AZ find themselves developing a vaccine that they supply at cost price - no profit. Their people have been working on this stuff for months, night and day, 24/7, and have found a vaccine at record pace and delivered it to the world. As a company, they do not deserve the heavy handiness of EU authorities raiding their Belgium sites to check AZ position.
As for UK fast approval, last year within the Transition period, Mutual Recognition agreement still held. For many years the MHRA was seen as the leading Medicines Licensing Authority in the world. The MHRA has consistently approved medicines on behalf of Europe for many years. The EU could have continued with this and approved the AZ vaccine on the back of the MHRA approval 4 weeks ago. They chose not to.
The MHRA approved quickly, as under new UK emergency legislation, data from trials was delivered to the MHRA in almost real time, and was being assessed very quickly. In the EU, all data was delivered to them at the end of all the data collection - months later. Thats why the UK approved sooner. We were the leading Medicines regulator in the EU and under Mutual Recognition, approved nearly 50% of Europe's medicines until Brexit. It was why the European Medicines Authority (EMA) was based in London until Brexit.
And now, the EU are shutting the border in NI to prevent any EU produced vaccine getting into the UK!!! You couldn't make it up.
Legally, the EU have not got a leg to stand on.
Morally we would live with some friendly conversation and do a deal and give them some vaccine.
What a wonderfully constructed post - a thing of beauty! Just too good for this thread.
Respect from Lingfield to Lindfield.