Participation in medical research

We always conduct our clinical studies with respect for the fundamental and human rights of citizens, on a fully voluntary basis, and in compliance with good research practice. All our studies must be approved by the Ethics Committee and be granted a research permit. HUS Ethics Committees issue opinions on medical research conducted on humans and human embryos and fetuses in the Uusimaa region. The ethics committees attend to the interests of the test subject.

Clinical trials are an essential part of the development of new medicines and further research into existing medicines. Participation in clinical trials is a patient's prerogative in a university hospital. As a research patient, you will have access to innovative treatments as much as several years before the general public, besides having your health monitored and gaining experience of what it is like to be examined for research.
For a seriously ill person, participating in a clinical trial may give them a second chance. As a patient participating in clinical trials, you are covered by the HUS indemnity insurance and protection on the same grounds as other patients.

In order for the study to obtain the favorable opinion and permission of the Ethics Committee,

• the participant in the study must be requested to provide an informed consent to participate in the study,
• the study must comply with the legal requirements for the protection of the research subjects,
• the study must have the resources necessary to carry it out,
• the data protection of confidential data in the study must be safeguarded as required by law,
• the research financing plan must cover the costs it incurs on the hospital district, and
• the code key of the study must be retained in possession of HUS or someone acting in its behalf.

If you are interested in participating in research, you can send an email to:

Comprehensive Cancer Center research: unyhnaghgxvzhfcbgvynnxfv@uhf.svif.suh@iskaalitopsumiktutnaulah

MeVac trials: inppvar@uhf.svif.suh@eniccav
 

As a research participant, you have the right
 

• to access your personal data
• to give and withdraw your consent.
• to rectify your data
• to data erasure, or the right to be forgotten
• to restrict processing your data
• to object processing your data