FOR PATIENTS

FOR PATIENTS

A rich collection of information that every patient should be familiar with.

RESEARCH IN THE CENTER

The center and the doctor who is to conduct the clinical trial have to be accepted by the Bioethical Committee and the Central Register of Clinical Trials. After obtaining this acceptance, the research documentation flows to the center and all persons participating in the research: doctors, coordinators, nurses and lab technicians undergo training, depending on the scope of duties, regarding the test protocol, the test substance and medicines used, data collection and documentation .

All apparatus used in the study must have appropriate certificates.

After checking by the representative of the company the research, the center gets permission to include its participants in the study. The number of participants in a given study depends on the sponsor’s decision, determined by various factors.

Each participant, if they does not finish the study prematurely, on their own or researcher’s decision, they take part a specific number of visits (set out in advance).

After the last visit of the last participant and the collection and transfer of all medical data to the sponsor, the center’s study is closed. The center archives the history of the participants’ disease.
After completing the entire program, the center receives “blinding” data, which is made available to former participants of the study. They are important for the assessment of individual reactions to medicines and may influence the future decisions of doctors as to the choice of therapy.

CONTACT FORM FOR PATIENTS



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GENERAL INFORMATION

Centrum Badań Klinicznych PI-House Sp. Z o.o.
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Contact

ul. Na Zaspę 3, 80-546, Gdańsk

+48 58 719 22 22

pihouse@pihouse.pl

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