Skilled and Precise

Our studies are conducted by professionally trained staff, including doctors, nurses, pharmacists, etc. You can approach them with any questions—so please don’t hesitate to ask! Our centre is equipped with all the necessary medical devices, just like a hospital.

How we conduct a study is precisely outlined in the study protocol. You can think of it as the script for a film. You will receive a lot of information about the clinical trial from the study doctor, both verbally and in writing. At any time during the study, you can ask the doctor for additional explanations. 

 

Legislation

J&J CPU complies with all (inter)national regulations regarding clinical research. These rules ensure that the safety of a participant is always a priority and that participation is voluntary. You are never obligated to participate; it is always your choice. At any time, you have the right to withdraw from the study. Additionally, all our studies must be pre-approved by an independent ethical committee.

 

Risks

No treatment is without risk. Registered medicines (medications that are already on the market) also have their side effects. The study doctor is required to inform you of everything known about the potential risks. Before deciding to participate, you can always weigh the pros and cons.

Not all side effects of a medication can be predicted in advance. However, doctors can estimate which side effects may occur based on prior research. The new medication has already undergone extensive testing in the laboratories of pharmaceutical companies or academic centres. Only when the results are very favourable do we proceed to research in humans.

During the study, doctors and nurses will closely monitor the volunteers. If new data emerges during the study, both positive and negative, the doctor will inform you as soon as possible, and the study may be adjusted if necessary. 

 

Insurance

Researchers strive to prevent anything from going wrong during the study. The ethical committee and the FAMHP also ensure that measures are in place to avoid potential harm from the research. The company organizing the study has taken out insurance that provides coverage in case you experience any harm as a result of your participation. Such harm will be compensated in accordance with legal provisions.

In exchange for your contribution to drug development, you will receive compensation. The amount is determined based on the duration of the study and the number of outpatient visits. No consideration is given to the risks or possible side effects of the study medication; it is purely compensation for your time and commitment.