FOR PATIENTS

FOR PATIENTS

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

SUPERVISION OF A RESEARCH IN THE COUNTRY

Before granting permission for conducting a clinical trial in our country, the Ministry of Health submits them to the Office of Registration of Medicinal Products, Medical Devices and Biocidal Products, the Central Register of Clinical Trials (CEBK) that controls the compliance of audit documentation with legal standards.

After the consent for conducting the study has been granted, already during its duration the CEO of the said Office has the possibility of controlling the research by the help of the Clinical Trial Inspection; among other things, the application of the Good Clinical Practice standards, compliance of the test with the protocol, correctness of record keeping, etc.

Throughout the study, the Central Bioethics Committee also has insight into it, gathering information about side effects that occurred with its participants, analyzing any changes to the protocol and other documents determining the way the research, thus ensuring the safety of the participants.

CONTACT FORM FOR PATIENTS



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Consent II - I agree to receive information on my e-mail address or my mobile phone number from Centrum Badań Klinicznych PI-House Sp. z o.o. with headquarters in Gdańsk (80-546), ul. Zaspa 3 commercial information by e-mail.

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GENERAL INFORMATION

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

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+48 58 719 22 22

pihouse@pihouse.pl

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