Full-service clinical trial management across every phase of research — from protocol design to publication.
MD TRIAL provides end-to-end clinical trial coordination, supporting every phase of research — from protocol design and site selection to data lock and final reporting. Our experienced project managers ensure that studies are delivered on time, on budget, and in full regulatory compliance, maintaining transparent communication with investigators, sponsors, and regulatory bodies throughout the process.
Our regulatory affairs specialists manage all submissions to national authorities and ethics committees, ensuring compliance with GCP, MDR, ISO 14155, and local regulations. We assist in protocol and informed consent review, device classification, clinical evaluation plans, and communication with competent authorities to streamline study approval and execution.
We offer comprehensive on-site and remote monitoring using a risk-based approach to ensure patient safety and data integrity. Our secure electronic data capture (EDC) systems provide real-time access to study data, supporting efficient query resolution, audit trails, and regulatory readiness.
Our biostatistics team delivers robust study designs, statistical analyses, and data interpretation that meet both scientific and regulatory expectations. We provide protocols, statistical analysis plans (SAPs), clinical study reports (CSRs), and peer-reviewed manuscripts, ensuring clarity, accuracy, and publication readiness. Medical writers collaborate closely with investigators to translate complex results into compelling, evidence-based narratives.
MD TRIAL integrates health economics and real-world outcomes research to demonstrate clinical and economic value. We develop cost-effectiveness and budget impact models, conduct comparative effectiveness analyses, and generate evidence to support market access, reimbursement, and value-based healthcare decisions.
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