EU must put human-relevant science at heart of pharmaceutical strategy
Our recommendation to Commission consultation assessing impact of Europe’s pharmaceutical legislation
We have submitted to the Commission's impact assessment of the review of EU pharmaceuticals laws, calling for action on animal testing and adoption of human-relevant test methods to improve the efficiency and efficacy of medicines development.
As part of the EU pharmaceuticals strategy, and drawing lessons from the COVID-19 pandemic, the Commission is reviewing EU legislation on medicines for human use to make it future-proof and crisis-resistant. The evaluation aims to ensure access to affordable medicines, cut red tape and foster innovation for new scientific and technological developments.
To achieve the goal of safe and affordable medicines and to support the European pharmaceutical industry to innovate and make the most of existing alternatives to animal tests which consistently fail to deliver human health breakthroughs, we are recommending that the EU:
"90% of drugs fail in clinical trials on humans despite having passed pre-clinical studies, including extensive tests in animals."
- Places humane and human-relevant preclinical assessment at the heart of its strategy.
- Moves away from the current outdated and unreliable animal testing paradigm.
- Prioritises investment in modern and human-relevant methods.
- Sets targets to phase out animal testing.