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Healthy Volunteers, Patient Participants and Special Population
ALS
clinic meets the ICH criteria while convenient for the long
stays. Please
click link1
and link 2 to
view the facilities where you volunteers stay when participating
in clinical studies.
We start recruiting volunteers (either healthy or patient) in
clinical studies only when the study protocol has been approved
by the IRB qualified Ethic Committee. Its experts ensure the
clinical study does not compromise the safety and the rights
of participants are protected.
After the participants have been informed about the study objectives,
rules, potential side effects, their rights and obligations,
if they express interest in participating they first sign an
informed consent for medical screening that involves medical
tests and face-to-face interview. The tests are performed at
ALS facility at no cost (to participants).
The recruitment, the screening and the stay for participating
in the study occur at the same place.
- We accommodate volunteers with all what they need during the
confinement.
- The meals are prepared on site and served on time as scheduled.
In some studies the medication is administered under fed conditions
which mean volunteers receive it after a-high or a low fat breakfast.
- Volunteers are requested to complete 100% of the meals served.
- We do not have a smoking room or area which means only light-smokers
(if allowed) or nonsmokers can participate. |
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