Clinical Study Management

At mediSMART, we provide end-to-end clinical study management services tailored to support sponsors throughout the entire trial lifecycle. Our experienced team ensures operational excellence by combining scientific insight, regulatory expertise, and streamlined processes.

Our Clinical Study Management services include:

📄 eCRF and ICF Design, Adaptation, and Implementation

We design and implement customized electronic Case Report Forms (eCRFs) and Informed Consent Forms (ICFs) that are aligned with global regulatory standards and tailored to protocol-specific needs. Our team ensures that forms are user-friendly, compliant, and optimized for high-quality data collection.

🧪 Local and Central Laboratory Organization

We coordinate local and central laboratory services, ensuring efficient sample logistics, standardized data reporting, and compliance with country-specific requirements. Our established lab networks and vendor oversight practices reduce delays and improve data consistency.

🎓 Study-Specific Trainings

We develop and deliver customized training programs for investigators, site staff, and study teams. Our trainings cover protocol procedures, GCP compliance, and system usage, empowering teams with the knowledge and tools they need for successful execution.