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To better assist you with your request, please choose a research area provided by Southern Clinical Research Group. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Clinical Protocol Design & Development

Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is maintained as well as maintaining the integrity of the data collected during the trial.
Real-World Evidence

Acquire clinical data from patients' medical records to analyze trends and the frequency of occurrence of different medical conditions.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Patient Recruitment

Recruit and retain patients for clinical trials.
Real-World Data

Acquire real-world data from patients' electronic medical records including clinical information generated during the course of healthcare.
Database Management Software

Facilitate the collection, tracking and processing of biological facts, statistics and observations.
Clinical Trial Recruitment

Recruitment, enrollment and retention of patients for clinical trials.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Study/Site Feasibility Study

Explore and test study practicality.
Investigator Recruitment

Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
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