Ensuring CTR compliance, GCP standards, and acting as EU sponsor contact for drug clinical trials.
Providing MDR compliance, ISO 14155 alignment, and regulatory liaison for medical device clinical investigations in Europe.
Ensuring CTR compliance, GCP standards, and acting as EU sponsor contact for drug clinical trials.
Providing MDR compliance, ISO 14155 alignment, and regulatory liaison for medical device clinical investigations in Europe.
Appointing a trusted EU Legal Representative is essential for non-EU sponsors starting drug or medical device studies in Europe. At GCP-Service, we go beyond the “post box” role, ensuring compliance with EU CTR and MDR, streamlining regulatory submissions, and providing expert guidance for smooth trial execution. Partner with us for reliable representation and added value in every step of your clinical research journey.
We support sponsors across all EU member states and the UK. Our experts ensure compliance and smooth clinical trial execution from start to finish.
We deliver cost-efficient EU representation for drug and device studies. With 12 completed studies and repeated business from global sponsors, we are a proven long-term partner for successful trials in Europe.
Beyond representation, our team ensures ongoing compliance with EU CTR, MDR, and GDPR standards, supporting you in keeping your studies inspection-ready.
Contact us for expert guidance!
Contact us for expert guidance!
