CRO Services - ACTG-CRO

Site Management Organization (SMO)

We keep our processes and your projects under control through the implementation and oversight of our in-house, updated, precise Standard Operating Procedures (SOPs) or the Client’s SOPs if this is your preference.

ACTG-CRO provides SMO to help support both principal investigators and sponsors.

 

Through our SMO service, we provide principal investigators with trained CRAs II to assist with daily clinical trial activity and patient recruitment; and sponsors to provide clinical trial site management and ethics committee support.

We plan the studies and organize the meetings of the investigators in our offices or at the Investigator's or in the place defined by the Study Promoter.

Site Management Organization Services include:

  • Study Management

  • IRB Management

  • Site contract, budget expense management

  • Enrolling and retaining participants, managing visits

  • Patient safety management

  • Safety and Adverse Events (AEs) Management

  • Ensuring Protocol Adherence

  • Ensuring Data Security

  • Quality control

  • Logistics management

  • Archiving Essential Documents

  • Archiving trial data

  • Data Collection

  • eCRF completion

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.

  • Twitter
  • LinkedIn Social Icône