How bold can Europe be? Delivering on the Biotech Act for clinical trials

As legislators review the Biotech Act, they face a generational opportunity to strengthen Europe’s clinical trials landscape and its global competitiveness.

The Commission’s proposal outlines changes that can help reverse Europe’s declining share in global clinical research, bridge the emerging competitiveness gap, and enable a faster, patient-center and more ambitious approach to clinical trials, while maintaining the EU regulatory standards.

Bringing together policymakers and stakeholders, this discussion will examine how the proposal can deliver on these ambitions and identify key elements ahead of upcoming negotiations. It will also explore perspectives from EU Member States that are leading in clinical trials.

This event is by invitation only.

Interested in this event?

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Guiding questions include but are not limited to:

• What are the key elements of the Biotech Act that can modernize Europe’s clinical trials landscape?
• How bold can Europe be in advancing clinical research amidst global competition?
• How do some Member States, such as Spain, lead on accelerating clinical trials and what positive impact this has on patients and innovation?
• How can momentum from the Commission proposal be maintained ahead of upcoming negotiations, and which core elements of the proposal must be safeguarded during negotiations?

Health Editor
VitalSigns.news
(Renew, Denmark)
European Parliament
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