Regulation & Guidelines
Helsinki Committee
Kineret follows the guidelines and regulations of the Ministry of Health in providing access to medical information for researchers and entrepreneurs.
The role of this committee is to ensure the rights, safety, and welfare of participants in a clinical trial, by examining and approving the clinical trial’s protocol and informed consent form. The committee is also responsible to regularly monitor the course of the trial, as well as all changes to the protocol and informed consent form, and to supervise the clinical trial.
Helsinki subcommittee – Research on existing data
The Helsinki subcommittee is responsible for approving research that is not a clinical trial in humans. The subcommittee discusses research proposals for collecting information from patients’ medical, nursing, etc. records without involving the patients.