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Japan’s Emperor Naruhito to make historic Belgium visit marking 160 years of diplomatic ties

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Japan’s Emperor Naruhito to make historic Belgium visit marking 160 years of diplomatic ties

Japan’s Emperor Naruhito to make historic Belgium visit marking 160 years of diplomatic ties Japan’s Emperor Naruhito to make historic Belgium visit marking 160 years of diplomatic ties
  Japan’s Emperor Naruhito and Empress Masako will travel to Belgium for an official visit on 23 and 24 June, commemorating 160 years...
Read More...

EU agri-trade hits €24.7 billion surplus despite trade headwinds

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  The European Union’s agricultural sector maintained its status as a global powerhouse in 2025, posting a €24.7 billion trade surplus...
Read More...

Dutch confidence in politics sinks to record low as public trust erodes

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  Public trust in Dutch politics has fallen to its lowest point in more than a decade, according to new figures released by Statistics...
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EU border refusals rise as deportations increase in 2025

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EU mobilizes emergency response to hantavirus outbreak on cruise ship

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Age bias tops list of discrimination complaints in Flanders, new study finds

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  Marking a decisive shift from a decade of crisis management to long-term nation-building, the European Commission and the Syrian Transitional...
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Poland leads global surge in ultra-wealthy population as economy booms

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  Poland has recorded the fastest growth in the world in the number of ultra-wealthy individuals over the past five years, according to...
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EU services sector hits speed bump in February despite annual growth

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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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