European Commission vice president Maros Sefcovic has told political group leaders in the European Parliament that technical discussions with the UK on the Northern Ireland Protocol are progressing and that the UK was engaging on the issues “in good faith.”
2/ Two sources have also confirmed that Mr Sefcovic’s UK opposite number Lord Frost has accepted an invitation to travel to Brussels for dinner with Mr Sefcovic on Thursday evening.
3/ It’s understood Mr Sefcovic told the European Parliament’s Conference of Presidents, made up of the political group leaders, that while technical talks on the Protocol were proceeding positively, there were some 27 issues which remain outstanding.
4/ He downplayed expectations that there would be a breakthrough between both sides in the short term.
5/ “On most of the issues [vice president Sefcovic] believes they can conclude them on a technical level but obviously there are certain political things that are outstanding,” said a source present at Mr Sefcovic’s briefing to the Conference of Presidents.
6/ A UK govt spokesperson said: “Technical engagement with the EU in relation to the Protocol has continued over recent days and we remain in regular contact at all levels. The discussions have been constructive but there are still significant differences that need to be resolved
7/ “Both the UK and EU are engaging with business, civil society and other stakeholders in NI, to understand the issues they are facing.
8/ “The UK remains committed to working through the outstanding issues in order to restore confidence on the ground in Northern Ireland , reflect the needs of communities and respect all dimensions of the Belfast Good Friday Agreement.”
9/ Meanwhile two European Parliament committees are expected to vote this week to give their consent to the EU UK free trade agreement, concluded in December.
10/ However, the Conference of Presidents has deferred a decision on when the Trade and Cooperation Agreement (TCA) should face a consent vote by the Parliament as a whole.
11/ The next plenary session of the European Parliament will take place on April 26-29. The Conference of Presidents will decide next Thursday whether or not to put the Parliament’s consent vote on the agenda of that plenary session.
12/ The TCA is currently being applied provisionally, and cannot be fully ratified until the European Parliament gives its consent.

A plenary vote on consent has been held up due to concerns by MEPs over the UK’s move to unilaterally interpret the Protocol.

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More from @tconnellyRTE

14 Apr
BREAKING: The United Kingdom has asked for more time to respond to the legal action taken by the EU over it’s unilateral decision to ease the requirements of the Northern Ireland Protocol, @rtenews understands.
2/ The request came in two letters from the UK’s chief Brexit minister David Frost. The EU launched twin-track legal proceedings against the UK on March 15 following the decision by the NI Secretary Brandon Lewis to unilaterally delay the full implementation of the Protocol.
3/ The Commission had issued a letter of formal notice to the UK government, which is the first step in a legal procedure which could end up in the European Court of Justice.
Read 9 tweets
24 Mar
On the eve of the EU video summit tomorrow, plenty of briefing on vaccines, so here is a guide to some of the sentiment out there:
1/ The European Commission's new vaccine export restrictions will be discussed by leaders but the reality is that under EU trade rules the Commission has a prerogative to amend regulations in this way...
2/ There is a growing number of leaders who will voice their concern at a restrictions leading to a lose-lose tit-for-tat vaccine trade war, and reputational damage for the EU. Ireland, NL, Sweden, Belgium and others in this camp
Read 13 tweets
24 Mar
Main points of the European Commission's new vaccine export restrictions:
1/ On top of the Jan 29 transparency mechanism, ie whereby member states must grant an authorisation to vaccine exports outside the EU to ensure they're compliant with EU vaccine contracts, there are added criteria
2/ Proportionality: roughly speaking, how much of the recipient country has already been vaccinated and what is the epidemiological situation in that country
Read 12 tweets
23 Mar
Worth noting by Sandra Gallina, EU's chief vaccine negotiator: last year the Commission entered advanced purchase agreements with pharma companies, ie buying doses of vaccines which did not yet exist.
2/ In order to conclude the contract the pharma companies needed a commitment of a certain amount of doses, ie an incentive to research + produce, so they would need a commitment to produce 300m doses for example
3/ However, as the negotiator, the European Commission needed to be sure the doses were being bought by member states. At the beginning, member states had to decide whether to stay in or out of the programme.
Read 7 tweets
22 Mar
Ireland's Minister for Foreign Affairs @simoncoveney says if the UK delivers a clear road map setting out how it will implement the NI Protocol, then the atmosphere would change and the EU would be in a position to “look at” flexibilities and extensions to grace periods.
2/ Coveney was speaking in Brussels after meeting the European Commission vice president @MarosSefcovic, co-chair of the EU-UK Joint Committee.

Mr Coveney said there had been contacts between EU and UK officials with a view to resuming more formal talks around the Protocol
3/ “I think certainly the EU side wants to get a process underway again so that both sides are talking to each other,” he told @rtenews
Read 11 tweets
16 Mar
Peter Arlett EMA: "If we look at what we would expect in the European population for thromboembolic events the number of reported events is far lower than we would expect in the background population
"The review is focusing on a small number of case reports of very rare + rather unusual thrombotic events, including thrombosis combined with thrombocytopenia. When you get down to individual cases,1, 2, 3 or 4 cases - then the epidemiological approach becomes much more difficult
"firstly it becomes difficult to get the background rates, there is less published in the literature, there is less available in electronic health care databases, therefore the focus is much more on looking at the clinical features of the individual reported case..."
Read 6 tweets

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