HOW DO WE GET INVOLVED IN THE CLINICAL TRIAL?
SERVICES PORTFOLIO
Writing of other study documents
Writing of other study documents
Writing of the Researcher's Manual, Information Brochure or Technical Sheet.
Economical Memory of the Trial
Economical Memory of the Trial
Economic Report of the Trial approved by all parties.
Regulatory Affairs
Regulatory Affairs
Drafting of ICF / HIP and submitting to CEIm and AEMPS (CTIS Platform) for approval.
Selection of Sites
Selection of Sites
Selection and contracting of Sites based on technical information in the CRO Database and in coordination with the Sponsor.
Selection of Radiopharmacy Units
Selection of Radiopharmacy Units
Choosing and establishing contracts with Radiopharmacies.
Transportation of radionuclide generator
Transportation of radionuclide generator
Reception and Transportation of the radionuclide to the contracted Radiopharmacies.
Distribution of IMP
Distribution of IMP
Coordination and distribution of the IMP (radiopharmaceutical) to Sites.
EDC Contract and e-CRF Design
EDC Contract and e-CRF Design
Contracting of the EDC and training of the Sites
