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EU-funded NGO linked to online map targeting Jewish and Israeli-affiliated businesses in Catalonia

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EU Parliament opens January plenary with support for Greenland

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Zurich introduces Eruv, creating a Sabbath-friendly public zone for Jewish life

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Germany warns AI-generated Holocaust images are distorting history

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European Parliament leaders back Greenland and Denmark, reject any challenge to Arctic sovereignty

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EU-funded NGO linked to online map targeting Jewish and Israeli-affiliated businesses in Catalonia

EU-funded NGO linked to online map targeting Jewish and Israeli-affiliated businesses in Catalonia EU-funded NGO linked to online map targeting Jewish and Israeli-affiliated businesses in Catalonia
  An online platform that mapped Jewish-owned businesses, schools, and Israel-linked companies across Catalonia has been linked to promotion...
Read More...

EU Parliament opens January plenary with support for Greenland

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  The European Parliament opened its 19–22 January plenary session in Strasbourg with a solemn tone, as President Roberta Metsola led...
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Zurich introduces Eruv, creating a Sabbath-friendly public zone for Jewish life

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  Zurich has quietly drawn a new kind of line across the city — one that cannot be seen at first glance, yet carries deep religious and...
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Germany warns AI-generated Holocaust images are distorting history

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EU asylum applications fall sharply in October 2025, even as repeat claims surge

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Princess Elisabeth takes on growing diplomatic role with NATO and EU leaders

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  Princess Elisabeth is steadily stepping into the international spotlight as part of her preparation to one day become Queen of Belgium....
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European Parliament leaders back Greenland and Denmark, reject any challenge to Arctic sovereignty

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As of Monday 31 January,  the assessment and supervision of clinical trials throughout the EU will be harmonised, notably via a Clinical Trials Information

System (CTIS) run by the European Medicines Agency. On this date theRegulation on Clinical Trialswill enter into application. This Regulation will improve conducting clinical trials in the EU, with the highest standards of safety for participants and increased transparency of trial information.

Welcoming this important step, European Commissioner for Health and Food Safety, StellaKyriakides, made the following statement:

“The Clinical Trials Regulation marks an important and positive step for European patients and brings us closer to a stronger European Health Union. It will allow us to have swifter authorisation of clinical trials across our Member States, thus improving the efficiency of clinical research as a whole. At the same time, the high quality and safety standards already set for such trials will be upheld. While almost 4000 clinical trials are already carried out each year in the EU, the Regulation will make vital research even more beneficial to the researchers and patients who depend on fast and reliable trials the most.

Over the coming years, the Regulation will create a framework for a more agile clinical trial approval process that will bring Member States closer together in the area of clinical trials. In turn, this will inspire further confidence and trust among citizens, who are at the centre of clinical research. This is why the Regulation is based on the key principle of transparency, allowing for public scrutiny at every step of the way.

I thank the Member States and the stakeholders who all worked closely with us to implement the new regulatory framework for clinical trials in Europe. I am also grateful to the European Medicines Agency, for not only their work on the Regulation, but also for their support in setting up the Clinical Trials Information System that will represent a single entry point for submitting clinical trial information in the EU.”  Photo- Ceescamel, Wikimedia commons. 

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