ITClinical's consultancy services can save you time and resources in a number of critical areas of the clinical trial process.
We can offer you great help with the Study Design, not only with the writing of the essential documents and the design of the EDC system for data patient collection according with the study protocol but also the Project Management, essential to ensure the timeline is being fulfilled, the recruitment happens as excepted, the external companies needed during the trial are coordinated and all the necessary activities to make sure that everything in the Clinical Trial is happening without problems.
Another important service that we can offer you is Data Management, designing the database, CRF discrepancy resolution and introducing the patient data in the database by single or double entry.
Pharmacovigilance and Training
We can take care of all the Pharmacovigilance issues from your Clinical Trial, such as risk management, SAEs reconciliation or preparation of periodic safety update reports.
Our team can prepare Training sessions in different fields such as Good Clinical Practice, study protocol, Clinical Trial procedures, Disease physiology or ITClinical's electronic systems.
Need something else?
Tell us about your needs! We'll be glad to help out.Contact us