Marketing on behalf of institution in order to increase number of trials;
Investigators team selection;
GCP trainings;
Feasibility questionnaires completion;
Contract negotiation;
Referral doctor involvement;
Investigator file review.
Data bases review;
Patient identification;
Patient visits planning and checking investigators availability;
IVRS;
(e)CRF completion and responses to queries IP record and distribution;
Investigator file management.
Clinical Development Plans;
Clinical Study Protocols;
Case Report Forms (CRFs);
Patient Medical History Forms;
Informed Consent Forms (ICFs).