CRO Services - ACTG-CRO

Coordination / Monitoring / Reporting / Central Remote Monitoring

The steering of the research is ensured by an Experienced Project Manager dedicated to the studied theme (realization and management of the TMF, coordination of the participants, regular communication with the Promoter of the study). The coordinating Investigator and/or opinion leader actively participates in the management of the study.

 

Our CRAs service ensures data quality, queries management and study monitoring by writing the plan and the report(s) of monitoring. It also supports the traceability of the tested products (drugs, medical devices ...).

We also propose for CROs companies worldwilde to Centralize their monitoring within our premise:

COST EFFICIENT SERVICES:

CENTRAL MONITORING FROM TUNISIA

 

 

100% Source Data Verification reviewed by our in-house CRA within our office in Tunisia through secure online workspaces.

BENEFITS OF CENTRALIZING THE MONITORING OF YOUR TRIAL WITHIN OUR PREMISES:

 

Advantages of remote monitoring/rSDV:

  • Increased accuracy

  • Detection of critical data and processes

  • Reduced time to submission

  • More focus to enhance CRA activities

  • Cost savings

  • Improved recruitment

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

Conducting your Clinical Trial at International Standards in Africa.

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