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

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