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Syntrial provides integrated services covering every stage of the clinical trial lifecycle — from study start-up to close-out.
Our flexible approach allows sponsors to choose full-service support or individual components tailored to their operational needs.
Study Start-Up
Efficient planning and initiation of clinical trials, including feasibility assessments, site selection, and regulatory submissions.
Our goal: fast, compliant study activation that aligns with both local and EU requirements.
Regulatory Affairs
Expert management of ethics committee and competent authority submissions, amendments, and renewals.
We maintain clear communication with local regulators to ensure accuracy and transparency throughout the approval process.
Clinical Trial Design & Management
Comprehensive trial planning, protocol development, and day-to-day coordination of clinical sites.
Syntrial oversees study timelines, budgets, and documentation to deliver quality data and on-schedule completion.
Clinical Monitoring
On-site and remote monitoring focused on data integrity, patient safety, and protocol adherence.
Our monitoring processes ensure compliance with EU and local regulations, GCP, ISO 14155:2020, and sponsor requirements at every step.
Project Management
Dedicated oversight of clinical operations, vendor coordination, and sponsor reporting.
We use structured communication and proactive risk management to keep studies on track.
Tailored Services
Every project is unique. Syntrial adapts its service models to fit your study structure, internal resources, and regional requirements — ensuring efficiency, transparency, and scientific integrity.
Specialized Support in Medical Device Studies
Proven expertise in clinical evaluation and performance studies for medical device trials.
We support MDR (EU 2017/745) and IVDR (EU 2017/746) requirements from study design through data analysis and final reporting.
Our in-depth knowledge and hands-on experience cover the full lifecycle of medical device studies — including first-in-human design, management, and close-out.
Contact us
Let’s discuss how Syntrial can support your next study.