Ethics Committee
CEIm
The Fundació Puigvert features an accredited Drug Research Ethics Committee (CEIm Fundació Puigvert IUNA), whose mission is to safeguard the ethical and legal principles of the research projects carried out.
It undertakes to ensure the safety of the patients participating in the different trials.
Contact persons
Technical Secretary of the CEIm: Beatriz Rodrigo (+34 93 416 97 00 ext. 4103
Useful information
Scope of action
We are the reference CEIm for dialysis centres.
Assessment requirements
(under construction)
Documents and forms
(under construction)
Standard Operating Protocols
The CEIm is accredited by the Department of Health of the Generalitat de Catalunya (Regional Government of Catalonia) to carry out its activities in accordance with its Standard Operating Procedures (SOP), which the CEIm uses to regulate its own internal operation.
The SOPs are reviewed on a yearly basis and are available to promoters upon request to the CEIm Secretariat.
*These procedures comply with current regulations (Royal Decree 1090/2015 of 4 December regulating clinical trials with drugs and the CEIms, BOE no. 307, 24/12/2015), and their content includes the aspects that are established in INSTRUCTION 1/2017 of the Directorate General for Professional Organisation and Health Regulation of the Department of Health on the accreditation procedure of clinical research ethics committees as drug research ethics committees.
Scope of action
We are the reference CEIm for dialysis centres.
Assessment requirements
(under construction)
Documents and forms
(under construction)
Standard Operating Protocols
The CEIm is accredited by the Department of Health of the Generalitat de Catalunya (Regional Government of Catalonia) to carry out its activities in accordance with its Standard Operating Procedures (SOP), which the CEIm uses to regulate its own internal operation.
The SOPs are reviewed on a yearly basis and are available to promoters upon request to the CEIm Secretariat.
*These procedures comply with current regulations (Royal Decree 1090/2015 of 4 December regulating clinical trials with drugs and the CEIms, BOE no. 307, 24/12/2015), and their content includes the aspects that are established in INSTRUCTION 1/2017 of the Directorate General for Professional Organisation and Health Regulation of the Department of Health on the accreditation procedure of clinical research ethics committees as drug research ethics committees.