1. In order to begin the process of feasibility and start-up of the trial, the following documentation is required:
  • Conformity of the Service(s) involved completed (download model in available files) and signed by the head of the corresponding Area. The research team should provide this document to the sponsor for submission to the CEImFJD.
  • The detailed financial report (Excel document), specifying the procedures included per visit, tests and the complementary procedures, with their respective costs.

  • Letter of delegation from the sponsor to the company acting as CRO, notarised, or with the Apostille of The Hague when executed before a non-Spanish notary, in applicable cases.
  • In the event that changes are made to the initial contract, an Addendum to the contract will be signed, for which 500 euros will be charged as an Addendum management fee (addendum models). In the event that the Addendum is for changes in the trial budget, 1,000 euros will be charged.
  • Contract management and other costs
  1. Clinical Trial Contract Models Our Contract models CHANGES ARE NOT ALLOWED