Top clinical trial specialists

Sign up for the study!

We are in the OMS database:

ORG – 100046187

LOC – 100076194

Our location:

ul. P. R. Kaczorowskiego 7 lok. 50 U

15-375 Białystok

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We have specialized in conducting clinical trials since 2009, which has allowed us to gain a wealth of experience and select a professional
and highly qualified research team. Our patients are cared for by dermatologists, diabetologists, cardiologists, endocrinologists, rheumatologists, neurologists, internists and pulmonologists, as well as nurses and clinical trial coordinators.

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Why participate in clinical trials?

Among the biggest advantages are access to innovative treatments, remaining under constant, specialized, free medical care with access to advanced diagnostic methods rarely used in standard medical care.

If you would like to learn more about the projects we run, call or fill out the form!

Comprehensive patient support at every stage of the study

Ability to receive modern treatment

Access to a range of free specialized tests

Free treatment

Frequently asked questions

Clinical trials are conducted according to strict protocols and so-called patient inclusion and exclusion criteria. Only those who meet all the conditions for participation will be invited to participate in the study. Verification is carried out by a doctor on the basis of a detailed history and any additional tests.

Among the biggest advantages are access to innovative treatments, remaining under constant, specialized, free medical care with access to advanced diagnostic methods rarely used in standard medical care.

The use of any medicinal substance carries the risk of adverse reactions. However, to ensure maximum safety, the conduct of clinical trials is approved and monitored by the relevant government organizations – the Ministry of Health, the Bioethics Committee, the Central Register of Clinical Trials. When entering a trial, the patient has the opportunity to discuss with the doctor the risks associated with the use of the investigational product, is given information about its effects and the conduct of the entire clinical trial in which he or she wishes to participate, the so-called Informed Consent.

Participation in clinical trials is completely free of charge. There is no cost to the patient, he or she receives free specialized medical care and often, if the study requires it, free access to advanced diagnostics. Patients are also reimbursed for travel expenses to the Center.

A clinical trial participant may withdraw from participation at any time without suffering any consequences. He or she will not be charged for the treatment he or she received, nor will he or she have to pay any penalties. The doctor may ask the reason for withdrawing from the study to make sure the patient is sure of his or her decision.

Participation in a clinical trial can sometimes be more involved than traditional treatments. Patients are required to attend all scheduled appointments, and if they cannot make it, they should inform the Center by phone as early as possible. It is also imperative that the participant adhere to the doctor’s instructions, provide information about past illnesses, changes in health and any side effects he or she notices, if any.

Clinical trials can be sponsored by various entities, such as research institutes or foundations, and most often by pharmaceutical companies.