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Rima Hassan to stand trial in France over controversial X post linked to 1972 airport attack

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Russia expels last Dutch journalist Geert Groot Koerkamp, raising concerns over media freedom

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Belgium approves capital gains tax: key details, political divides, and what it means for investors

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EU tobacco rules cut smoking rates, but new nicotine products pose growing risk, Commission warns

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EU lawmakers press China on e-commerce fairness, safety, and market imbalance during high-level visit

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Rima Hassan to stand trial in France over controversial X post linked to 1972 airport attack

Rima Hassan to stand trial in France over controversial X post linked to 1972 airport attack Rima Hassan to stand trial in France over controversial X post linked to 1972 airport attack
French Member of the European Parliament Rima Hassan is set to face trial in July after posting a controversial message on social media that...
Read More...

NGO report claims violence and illegal pushbacks at Poland–Belarus border as humanitarian crisis deepens

NGO report claims violence and illegal pushbacks at Poland–Belarus border as humanitarian crisis deepens NGO report claims violence and illegal pushbacks at Poland–Belarus border as humanitarian crisis deepens
  A new report by the We Are Monitoring Association has raised serious allegations of abuse against migrants and refugees at the Poland–Belarus...
Read More...

Russia expels last Dutch journalist Geert Groot Koerkamp, raising concerns over media freedom

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  Russia has revoked the press accreditation of Geert Groot Koerkamp, effectively removing the last Dutch journalist reporting independently...
Read More...

Belgium approves capital gains tax: key details, political divides, and what it means for investors

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  Belgium’s Chamber of Representatives has formally approved the introduction of a long-debated capital gains tax, marking a significant...
Read More...

EU tobacco rules cut smoking rates, but new nicotine products pose growing risk, Commission warns

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  The European Commission has published a comprehensive evaluation of the European Union’s tobacco control framework, concluding that...
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Belgium urges caution over energy supplies amid Middle East tensions

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  Belgium’s Foreign Minister, Maxime Prévot, sought to calm public concerns over energy security on Thursday, emphasizing that while...
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Booming caravan holidays in the EU: 413 million nights spent in 2025 as outdoor tourism surges

Booming caravan holidays in the EU: 413 million nights spent in 2025 as outdoor tourism surges Booming caravan holidays in the EU: 413 million nights spent in 2025 as outdoor tourism surges
  As spring blossoms across Europe and sunlight hours stretch longer, thousands of holidaymakers have once again embraced life under canvas...
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EU unemployment rate 2026: euro area at 6.2% as youth joblessness edges higher

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EU lawmakers press China on e-commerce fairness, safety, and market imbalance during high-level visit

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  A delegation from the European Parliament’s Internal Market and Consumer Protection Committee has wrapped up a high-profile visit to...
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EU releases €1.4 billion from frozen Russian assets to boost Ukraine aid

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  The European Union has secured another €1.4 billion in revenue generated from immobilised Russian central bank assets, reinforcing...
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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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