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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

Clinical Data Management - Biostatistics -

ACTG-CRO data management team develops detailed specifications for the collection, organization, validation, and analysis, of clinical trial data that ensures the most cost-effective, secure, and regulatory compliant process. Among the services provided by our team:

Case Report Forms (CRFs) design
Clinical data review for errors and trends generates electronic queries
Data entry
Serious Adverse Events reconciliation
Clean Data base analyzable
Protocol Review
Power calculations / Sample size
Statistical analysis

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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