Climate change and energy emissions

EU clean energy transition

Under the European Green Deal, the EU has set ambitious targets to reduce its greenhouse gas emissions progressively up to and beyond 2030 with the ultimate aim of reaching net zero emissions by 2050. The European Green Deal—tracker tracks policy developments at the EU level under the European Green Deal, central to which is the commitment to make the EU the first climate-neutral continent by 2050.

To achieve this, the EU is currently developing and implementing a legal and policy framework for a climate neutral, ‘clean’, energy system, centred around renewable electricity and renewable hydrogen coupled with improved energy efficiency. The EU clean energy transition—outline outlines the various limbs of this clean energy transition framework. This outline forms an introduction to a suite of detailed content on the clean energy transition, comprised of the following Practice Notes:

  1. EU clean energy transition—energy system integration—this Practice Note tracks the progress and implementation of the key actions contained within the Commission’s strategy for energy system integration, launched in 2020. The Commission’s intention is that the EU strategy on energy system

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Commission publishes updated clinical trials guidance package

The European Commission's Directorate-General for Health and Food Safety has published a comprehensive package of updated clinical trials guidance documents, all endorsed by the Clinical Trials Coordination and Advisory Group (CTAG) on 15 October 2025. The package includes new recommendations on criteria for selecting a reporting Member State under Article 85(2)(c) of the Clinical Trials Regulation, establishing a workshare criterion when proposed reporting Member States decline the role, which occurs in approximately 30% of applications. The Commission has updated its recommendation paper on decentralised elements in clinical trials (Version 02), superseding the December 2022 version, with revised national provision overviews and guidance on informed consent, investigational medicinal product delivery, and remote monitoring. A new recommendation paper addresses frequent issues identified during Part I and Part II assessments, based on feedback from national competent authorities and ethics committees, covering investigational medicinal product dossiers, protocols, and safety reporting. The package also includes revised guidance on auxiliary medicinal products, effective 1 December 2025 for new applications, featuring an updated classification system distinguishing between authorised, modified authorised, and unauthorised auxiliary medicinal products with corresponding application and safety reporting requirements.

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