Management of the Suitability of the Facilities
In order to start a clinical trial, it is necessary to request the signature of the suitability of the facilities by sending an e-mail to the INCLIVA Clinical Trials Unit (ensayosclinicos@incliva.es) with the basic data of the study (Code, EUDRACT, Principal Investigator and Conducting Service) and the following documentation:
- Study Protocol
2. Synopsis in Spanish.
- General Economic Report
4. INCLIVA Suitability Model Facilities Annex IV AEMPS completed.
Upon receipt of the application, INCLIVA Clinical Trials Unit will contact the Principal Investigator and his team to confirm the participation of other services involved and will proceed to process the signature of the document by the Medical Management of the Centre (the only valid signature for the suitability of the facilities).
The Clinical Trials Unit will send the signed document to the Sponsor or CRO at the requesting e-mail address and the management of the contract and the financial report can begin.
Facility Suitability Management
Manu Erasun
ensayosclinicos@incliva.es / merasun@incliva.es
Phone: 961 62 89 21
Contracts and addenda
Invoicing
Mayca Román
facturacioneecc@incliva.es / mroman@incliva.es