European Legislation & Regulation
Advancing industry interests in European legislation and regulation
ACRO’s European agenda is focused on advancing policies that foster innovation and harmonization.
ACRO engages with regulators and policymakers in the EU and UK to ensure a positive regulatory and business environment that supports high-quality, safe, and ethical clinical research – including the European Commission, the European Medicines Agency (EMA), and the UK Medicines and Healthcare products Regulatory Agency (MHRA), and the EU national competent authorities. In addition, ACRO engages with data protection regulators, such as the European Data Protection Supervisor (EDPS), to promote appropriate privacy and data protection regimes that protect data subjects and also facilitate research.
Contact us for more information about our European advocacy.