Clinical Trials


Clinical research: professional and transparent


With a mandate from the Universitätsmedizin Göttingen (UMG), we promote the professionalization of clinical trials using our a results-oriented, patient-focused approach to conducting trials. IFS staff supervise and manage all clinical trials registered with the UMG. Our aim is to make clinical research practices more transparent to the patient, and ensure the process is fully understood.

Registering clinical trials

The registration and supervision of IITs and contract research trials is mandatory, and our practices comply with the Higher Education Act of Lower Saxony.

Once the online registration has been completed:

  • the trial will receive a unique ID number.
  • we will get in touch with you to discuss the next steps.
Get online registration form

More

Numbers and Facts

The focus of studies overseen by the IFS:

  • > 80 phase III trials
  • > 50 phase II trials
  • < 10 phase I and phase IV trials
Of these are:
  • 65%: AMG-trials
  • others: MPG-and preclinical trials
The trials are based predominantly in the following clinical departments::
  • Cardiology and Pneumology
  • Hematology and Oncology
  • Gynecology and Obstetrics
  • Neurology
  • Dermatology, Venerology and Allergology
  • Psychiatry and Psychotherapy


To learn more about registering trials with the IFS, please contact:

Anja Hernández – Head of Contract Management
Phone: ++49 (0) 551 - 39 - 175644
Fax: ++49 (0) 551 - 39 - 171344
E-Mail: hernandez.ifs@med.uni-goettingen.de


Mandy Dähling – Head of Budget Management
Phone: ++49 (0) 551 - 39 - 175643
Fax: ++49 (0) 551 - 39 - 171344
E-Mail: daehling.ifs@med.uni-goettingen.de