CEIC · Comitè d'Etica d'Investigació Clínica
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CEIC has diferents forms:

- IP Commitment
- IP-CEIC Commitment:
It refers to the obligations that the the IP has to the CEIC and it s the same for all the centres.

-Departments involved in Commitment : Pharmacy, Nursing, IDI, Laboratory and pathology.

These forms were agreed with the departments and the researchers of the hospital and the ICO.
The rest of the centres are not obliged to use these forms.

They remind, of the need to inform the departments involved in the study: of all those aspects to which the study relates, in particular the pharmacy department, but also nursing, laboratory, IDI or those who are involved.

Likewise, the sponsor and principal researcher in the centre have to inform the departments involved of the project's start up and completion.

In the case of researchers who do not belong to the University Hospital of Girona Dr. Josep Trueta put the LOGO CENTER REPRESENTED.
IP-CEIC Commitment
The responsibilities of the principal investigator in the relationship with the CEIC are:

1. To ensure that the CI will be collected according to RD1090/2015
2. To record in the clinical patients clinical history that the patient is taking part in a research study.
3. To ensure that all persons involved in the trial respect the confidentiality and protection of the patients personal data.
4. To inform the CEIC about of the study as required.
5. To facilitate the review of patient documentation in a clinical trial requested by the secretary of the CEIC.
6. To comply with all legal obligations made upon the investigator.
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