We provide support in time-consuming activities, helping the research team to reach the Project deadlines on time with full quality assurance.
- Clinical Trial Coordination: Our professionals are ready to support the research team, following its instructions and delivering results on time.
- Supporting the enrollment of subjects.
- Transferring of study data to the CRF, registering data and keeping updated all the research study tools.
- Attending monitoring visits, participating in the visits scheduled by the CRA, helping to solve discrepancies.
- Keeping updated the study files, such as Investigator Master File.
- Dealing with regulatory requirements, acting as contact person or representative.
- Writing and preparing all regulatory requirements before, during and at the end of the Study.