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EasyFeasibility
Try It. Test It. Trust It.

Smarter Site Selection. Faster Trials. Global Reach.

EasyFeasibility® is SynapCon’s digital gateway for selecting the right clinical research sites — fast, secure, and fully compliant. It replaces spreadsheets and email chains with a validated, cloud-based platform that lets sponsors and CROs pre-qualify, invite, and evaluate investigators worldwide in real time.

EasyFeasibility© gives you everything you need to identify, invite, and qualify the right study sites — globally, securely, and in record time.
Evaluate investigators, manage NDAs, and generate validated feasibility reports — all in one compliant environment.

✅ Compliant by Design: ICH-GCP, FDA 21 CFR Part 11, HIPAA, ISO 13485/14971
✅ Fast & Scalable: Cloud-based or on-premise deployment
✅ U.S. rollout supported by CyberActa

Experience the System Yourself

Ready to see how it works?
Visit our sandbox environment and explore EasyFeasibility© hands-on:
👉 https://feasibility.easyclin.eu/ctms-feasibility/

Learn how easy digital feasibility can be — and why teams trained on EasyFeasibility© deliver up to 60 % faster site selection and 40 % lower startup costs.

🎓 Get Trained – Become an Expert

Join our interactive online training sessions to:

  • Master digital feasibility workflows and reporting

  • Understand compliance and risk-based site qualification

  • Learn best practices directly from SynapCon specialists

📅 Register now or book a personal demonstration
👉 Book a Live Demo

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Why It Matters

Site feasibility is often where time and money are lost. EasyFeasibility® transforms this process into a standardized, digital workflow that:

  • Automates investigator outreach and data collection with built-in reminders and audit trails.

  • Generates instant feasibility reports with decision-support analytics.

  • Increases data accuracy and reduces non-response or incomplete submissions.

  • Ensures compliance with ICH-GCP, 21 CFR Part 11, ISO 13485/14971/27001, and EU/US privacy standards.

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Key Features

  • Global Investigator Network: Access a growing worldwide registry of qualified study sites.

  • Customizable Questionnaires: Define study-specific parameters while using validated templates for consistency.

  • Built-in NDA Handling: Integrated e-signature and confidentiality workflows protect sponsor data.

  • Regulatory & Risk Reporting: Automated feasibility summaries include KPI metrics and risk assessment indicators.

  • Secure Access Control: Role-based permissions, full audit trail, and GDPR/HIPAA compliance by design.

  • Cloud or On-Premise: Hosted and validated by our partners at Public Cloud Group  or deployable on secure in-house infrastructure.

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Benefits

  • Cut time-to-site selection by up to 60 % and feasibility costs by
    > 40 %.

  • Boost study quality and predictability through reliable site data and structured reporting.

  • Enable inspection-readiness from day one with built-in traceability and exportable XML audit files.

  • Empower collaboration between sponsors, CROs, and investigators — globally and securely.

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Powered by SynapCon | Operated in the U.S. by CyberActa

EasyFeasibility© is part of the EasyClin® Clinical Trial Management Suite, built and validated under ISO 13485 and IEC 62304.
Through CyberActa, U.S. customers benefit from localized hosting, regulatory alignment (FDA 21 CFR Part 11, HIPAA), and dedicated support for technology transfer and validation.

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