Key areas of interest

The EAU acknowledges the pivotal role that European Union regulation plays in the medical practice of its members.

Mobility of health professionals across the EU

The mobility of European medical practitioners within the continent has increased rapidly in the last decade. The EAU supports this by strengthening the network of European urologists and exchanging information and best practices.

Clinical trials regulation

Clinical trials are vital to the improvement of urological care. The new EU Clinical Trials regulation, applicable as of May 2016, stimulates clinical trials and seeks the highest standard for patient safety.

Medical devices legislation

Medical devices, from gauze to implants, are an integral part of urological practice and the quality and efficacy of urological care are enhanced by innovations in the sector.

The European Union seeks to ensure the highest level of patient safety, whilst maintaining competitiveness in the sector through regulation on market access, international trade and regulatory convergence.

Data protection legislation

The European Commission is revising the existing EU Data Protection Directive to ensure a more harmonized approach to data protection and privacy across the European Union. However, this could hinder research involving personal data, such as genetic research.

Regulation on advanced therapies

Advanced therapies, whether genetic, cell therapy or tissue engineering, have huge potential for urological patients. The EAU supports EU regulation designed to improve market access and foster competitiveness in the area of advanced therapy medicinal products that guarantee patient safety.

Education and training of medical professionals

Continuing Medical Education (CME) programmes are not implemented fully in many Member States. Adoption of urological guidelines and CME validation are key topics in which the EAU can contribute to policy improvements in this area.