AtACTG-CRO, we develop and maintain interactive relationships with the Study team and the Pharmacy of each Hospital/Investigating Sites, with the goal of efficiently processing safety data by keeping key people involved and coordinating communications to sites to limit redundancy. As a result, we get rapid identification of any potential safety issues and resolution of any open events.
Weare able to manage effectively safety data at the local, regional or global level both for investigational and marketed products. Wemonitor adverse events (AEs) encountered in clinical trials. Each safety event is reviewed in detail and sites are queried regarding discrepant information.
Clinical Research, Tunisia, Africa, Clinical Trials, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical