EU Health Data Regulation: Potential Risks to Medical Innovation

Monday, 4 August 2025, 02:08

EU health data law could stifle innovation in the pharmaceutical industry, warns Denmark’s pharma body. The regulation may weaken vital public-private research efforts.
Thepharmaletter
EU Health Data Regulation: Potential Risks to Medical Innovation

EU Health Data Law Raises Concerns

Danish pharmaceutical industry leaders have issued a stark warning regarding the new European health data regulation. This regulation is anticipated to hinder medical innovation while also potentially weakening collaboration between public and private research sectors. If these issues are not addressed, the EU could face setbacks in medical advancements that depend on robust data sharing and collaboration.

Impact on Research and Development

  • Increased Regulatory Burdens: The implications of the health data law may impose significant burdens on researchers.
  • Data Sharing Limitations: Access to essential data for innovative treatments could be restricted.
  • Collaboration Declines: The law may deter partnerships crucial for research breakthroughs.

Experts urge for a reassessment of the regulation to ensure it supports rather than hinders innovation in the healthcare sector.


This article was prepared using information from open sources in accordance with the principles of Ethical Policy. The editorial team is not responsible for absolute accuracy, as it relies on data from the sources referenced.


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