Range of Expertise and Services

Our Clinical Trials Center team offers a comprehensive range of services for conducting and managing clinical trials in accordance with international quality standards (ICH-GCP, AMG, MPG):

  • Trial planning and protocol development
  • Regulatory management (ethics, regulatory submissions, approvals)
  • Patient Recruitment and CareTrial Coordination and Monitoring
  • Data Management and Quality Control
  • Collaboration with Industry and Academic Partners
  • Responding to General Inquiries and Inquiries Regarding New Projects

With an experienced, interdisciplinary team of principal investigators, study physicians, study coordinators, and study assistants, we ensure that each of our studies is conducted to the highest scientific and ethical standards.

The entire, well-trained study team regularly completes continuing education (e.g., updates on GCP and IATA training, CPR courses, etc.) and participates in national and international conferences.

In addition, we offer:

  • High-quality, fully equipped separate laboratories with diagnostic equipment
  • Monitor stations and conference rooms
  • Sample processing and storage in refrigerators and freezers (-20°C, -80°C)
  • Trained staff for shipping in accordance with IATA and ADR standards
  • Emergency equipment
  • A 24/7 emergency hotline

Contact


Study Center Phone:
+49 (0) 40 7410 - 28532


Study Coordination Email:
infektionsforschung@uke.de


Address:
University Medical Center Hamburg-Eppendorf
Institute for Infection Research and Vaccine Development
Martinistr. 52
Building O10, 2nd Floor, PF 397
20246 Hamburg