Our Site Management Services (SMS) are designed to ensure the smooth execution of clinical trials, from site selection to study close-out. We aim to drive innovation and deliver results that make a significant impact on healthcare by supporting pharmaceutical, biotechnology, and medical device companies in conducting high-quality, compliant clinical research.
We offer various services to support site management in clinical trials, ensuring
efficient and effective conduct of research at investigational sites. Our key services for
site management include;
• Site Selection and Feasibility Assessments.
• Site Initiation.
• Clinical Trial Monitoring.
• Site Support and Training.
• Regulatory Compliance.
• Data Collection and Management.
• Quality Assurance and Audits.
• Site Closeout.
• Subject Recruitment and Retention Support.