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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.
Patient Recruitment

Recruit and retain patients for clinical trials.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Real-World Evidence

Acquire clinical data from patients' medical records to analyze trends and the frequency of occurrence of different medical conditions.
Database Management Software

Facilitate the collection, tracking and processing of biological facts, statistics and observations.
Real-World Data

Acquire real-world data from patients' electronic medical records including clinical information generated during the course of healthcare.
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.
RWE & RWD Study/Site Feasibility Study

Explore and test study practicality.
Regulatory Affairs Consulting

Receive assistance ensuring compliance with regulatory requirements.
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