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Conducting your Clinical Trial at International Standards in Africa and Europe.

Expanding your Business in Africa.

ACTG-CRO IS A GCP PROVIDER

Clinical Trials / Studies - Pharmaceuticals Marketing

Medical and Laboratory Equipment Supply - Training

Access Programs - Bioequivalence Studies - Business Expansion

CANCER REGISTRY PROGRAM

PHARMACOVIGILANCE

CF ACTG : Catalogue des Formations

CRO Services - ACTG-CRO

Pharmacovigilance

and Safety Reporting

At ACTG-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.

We are able to manage effectively safety data at the local, regional or global level both for investigational and marketed products. We monitor 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

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