We offer data management and statistical support tailored to early-phase clinical research. Services include CRF design, data validation, database lock, and statistical analysis planning. High data quality standards ensure accurate interpretation of safety and PK results. Our structured workflows support timely reporting and regulatory-ready outputs for early development decisions.
Ethics Committee approval for all studies
Medical supervision by experienced clinical staff
Clear participant information and informed consent
Conducted in compliance with ICH-GCP and EU regulations
