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Personnel and experience

If you are interested in participating in clinical trials please provide the following details.


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Potential principal investigator for clinical trials

The following contact data will be passed on in case of a feasibility enquiry. If you prefer other contact data to be passed on, please enter it below.
Principal investigator phone:
Principal investigator fax:
Principal investigator email:

Staff that are available for clinical trials

AvailableNumber Experience
in clinical trials
Subinvestigator
Subinvestigators' discipline / qualifications:
Study nurses / Study coordinator
Lung specialist
Cardiologist
Pharmacist
Physiotherapist
Radiologist
Nuclear medicine specialist
Neurologist
(Neuro-) Pediatrician
Psychologist
Psychiatrist
Ophthalmologist
Otorhinolaryngologist
Urologist
Internist
IT specialist
Laboratory personnel
Statistician

In addition to the patient population described before, can your centre recruit additional patients for clinical trials through cooperation with other medical centres for research?


Clinical Trials Experience

Are you familiar with the requirements of GCP (Good Clinical Practice)?

Have you had certified GCP (Good Clinical Practice) training?

Has your site participated in a clinical trial or observational study in the past two years?
If yes, in which phase?
If yes, how many?
For which indication(s)?

Are you currently conducting a clinical trial?
Please name the trial(s) you are currently conducting or have conducted in the past - and then click 'Add to list':
List of your clinical trials:

Does the study team have experience with IVRS (Interactive Voice Response System)?

Does the study team have experience with eCRF (electronic Case Report Form)?

Has someone of your study team experience with IATA (International Air Transport Association) packaging instructions?

Has your study team been audited for a clinical trial?
If yes, what kind of audit was it?



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