EasyISF :

The investigator-friendly solution to share documents with the sponsor.

Reduce the effort for monitoring visits and the burden for the study assistance. The commissioning can be ordered by the study sponsor at no cost to the study centre or as an internal clinic solution. The system is designed to cover all requirements from the strictest regulations in Europe (EU-GDPR), US (21CFR Part 11) and ICH-GCP E6 R2.
The EasyClin(c) project has received funding from the European Union’s Horizon 2020 research and Innovation programme under grant Agreement No 691546.
Your study will always remain inspection ready and let auditors perform large parts of their regulatory inspections remotely.
We offer either on-premises installations, cloud-based installations and flat rate options depending on your needs and budget.

Contact our sales team and schedule a demo.

The EasyISF solution is ideal to reduce the manual workload in studies, for both clinical staff and sponsors representatives: