Fill in the following form to receive methodological and/or statistical advice. An e-mail will be sent to you to confirm receipt and start the procedure for the requested service.
It is recommended that you apply well in advance as the service is subject to the availability of resources at any given time.
In accordance with the current General Data Protection Regulation (RGPD) and LOPD 3/2018, the sending of sensitive data is strictly prohibited and in case of non-compliance the documents received will not be accepted and will consequently be deleted. The principal investigator is responsible for compliance with the legislation.
Approval of the Research Ethics Committee (CEIm) is required
We inform you that any study, whether prospective or retrospective, that uses information relating to the health of individuals (clinical data, complementary examinations, analytical, radiological or imaging data, treatments, etc.) requires the approval of the Research Ethics Committee.
This is established by Royal Decree 1090/2015 for clinical trials, Royal Decree 957/2020 for observational studies with medicines and/or medical devices, and the Biomedical Research Act for all other research projects on human beings or biological material.
Remember that the request for approval from the Ethics Committee must be submitted at the start of the research, as the Committee does not make decisions on research that has already been carried out.