Our site selection process identifies high-performing sites based on experience, enrollment potential, infrastructure, and past performance, ensuring optimal study execution.

We manage all aspects of site initiation—from document collection and Local Ethics Committee and Regulatory Authority submission to site activation—ensuring a streamlined and timely start.

Our regulatory experts support submissions at local and international levels, ensuring compliance with current legislation and guidelines.

We offer both on-site and remote clinical monitoring services to ensure subject safety, data integrity, and GCP compliance throughout the trial.

Our team provides oversight and coordination, ensuring your study stays on track, on time, and on budget.

We deliver professional medical writing services for both pharmaceuticals and medical devices, including protocols, investigator brochures, clinical study reports (CSRs), and regulatory submissions.

Our data management services include database design, data entry, validation, and statistical analysis, ensuring accurate and reliable results.

We coordinate all aspects of transportation for study materials, biological samples, and investigational products, ensuring safe and timely delivery.

We provide certified translation of study documents, patient-facing materials, and regulatory submissions in multiple languages.

Our CRO acts as a strategic partner in sourcing and coordinating services, investigators, or study components based on your trial needs.

We handle contract negotiations and budget development with sites and vendors, ensuring favorable terms and cost-effective operations.

We offer expert legal and regulatory review of study-related documents to ensure clarity, compliance, and enforceability.

We manage procurement, storage, and distribution of medical supplies, including sourcing custom items based on specific study requirements.

We offer full-service clinical laboratory support, including acting as a Central Laboratory for your study. Our services cover sample processing, analysis, and result reporting with high standards of quality and turnaround