Site Management

MEDIKAPOLI CRO, provides pharmaceutical and medical device companies to conduct studies in sites provide the most accurate.
Researcher allows files up to date.
Patient files related companies will report after monitoring.
According to the study researchers will assist in the screening of patients.
Adverse event (AE) and serious adverse events (SAE) timely issues to be reported to the Ethics Committee and the Ministry of Health will support the center.
Drugs and medical devices stored in appropriate conditions in the centers will support centers.
Laboratory services will support in the center.
Set the dates for the visit of patients and patient support centers in a timely manner would come to visit.

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