ICE® is a software platform designed for electronic data collection, the creation of databases for Real-World Evidence (RWE) studies, and the efficient, intelligent, and seamless management of clinical data.
ICE® is a fully validated software compliant with industry regulations and guidelines (GxP-GCP, GAMP 5, FDA CFR 21 part 11 , EU Annex 11, MDR, GDPR, HIPAA) already used and validated by healthcare professionals in CROs, research organizations, pharmaceutical industries, scientific foundations, and hospitals in Italy and around the world.
Build your studies and significantly simplify the data collection process at reduced costs for clinical trials.
ICE® is a fully validated software compliant with industry regulations and guidelines (GxP-GCP, GAMP 5, FDA CFR 21 part 11 , EU Annex 11, MDR, GDPR, HIPAA) already used and validated by healthcare professionals in CROs, research organizations, pharmaceutical industries, scientific foundations, and hospitals in Italy and around the world.
Build your studies and significantly simplify the data collection process at reduced costs for clinical trials.
One ecosystem, multiple applications
ICE® can be integrated with the most advanced digital health solutions such as digital monitoring platforms, apps, medical devices, wearable devices, Software as a Medical Device (SaMD), and Digital Therapeutics (DTx).
Thanks to the use of API communications, ICE® can communicate with wearables and other apps to monitor vital signs, detect and record events.
It also integrates with other EDC systems and laboratory systems (LIMS).
Thanks to the use of API communications, ICE® can communicate with wearables and other apps to monitor vital signs, detect and record events.
It also integrates with other EDC systems and laboratory systems (LIMS).
ICE® Ecosystem is composed of the following products:
What they say about us
Preparation of ICE® for CDASH nomenclature developments and overall system performance optimization.
New section for drug management and optimization of existing features.
We are excited to announce the launch of ICE® ePRO, the innovative solution designed to transform clinical trial management by
The new version of ICE® eCRF introduces a dedicated section that allows users to select and export questionnaires to be
The latest update introduces several new features that improve study management, enhance security, and optimize data export. One of the
ICE is developed by:
Advice Pharma Group Srl