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Technology Solutions to Enhance the Performance of Your Clinical Trials

The digitization of clinical research relies on tools that are reliable, secure, and tailored to the sector’s regulatory requirements—ICH-GCP, CDISC, and 21 CFR Part 11.

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OUR APPROACH

Our teams combine proprietary solutions with off-the-shelf tools, integrated and configured to meet the specific needs of each project. From data collection to trial management and early access, this approach enhances the efficiency, traceability, and safety of your studies.
Each tool is configured according to the specifics of your protocol and can be integrated with your existing systems.

DATA COLLECTION

EDC: Reliable Clinical Data from the Moment It Is Entered

Our EDC (Electronic Data Capture) platforms replace paper-based case report forms with a secure eCRF. Your data is available for analysis in real time.

Custom eCRFs: forms configured according to the protocol, with automatic consistency checks during data entry.

Regulatory Compliance: audit trail, electronic signature, and validation in accordance with 21 CFR Part 11 and GCP.

HDS Hosting: Data hosted in an environment certified as a Health Data Host.

Tablet displaying an eCRF for data entry in a clinical trial

EDC
EDC Platform for Electronic Clinical Data Collection

CTMS Dashboard with tracking of sites, enrollments, and the clinical trial schedule

CTMS to Manage Your Clinical Trials

TEST MANAGEMENT

CTMS: Centralized Management of Your Clinical Trials

Our CTMS (Clinical Trial Management System) combines the operational, administrative, and financial management of your trials into a single tool.

Tracking centers and enrollments: site activation, patient recruitment, and monitoring visits—all visible at a glance.

Contract and Financial Management: Monitoring contracts, budgets, and payments to investigators.

Dashboards: Key Metrics and Alerts to Anticipate Delays and Meet Deadlines.

REMOTE MONITORING

Distantia, our remote monitoring platform

rSDV (Remote Source Data Verification): remote verification of source data, reducing monitoring time and the carbon footprint of monitoring.

Security and Compliance: Compliance with GCP, GDPR, and CNIL requirements for all data exchanges.

Operational Efficiency: Optimizing costs and timelines through technology tailored to decentralized design processes.

Monitoring: A remote monitoring platform

Distantia
: Real-time Remote Monitoring

EARLY ACCESS
: Centralized tracking, from application to enrollment

early access

ACCIOM, our solution for early access

Centralized management: tracking requests, from patient enrollment to treatment traceability, for early access and compassionate use programs.

Process automation: controlled transmission of orders and reporting of missing data.

100% web-based solution: accessible via a web browser and smartphone, hosted in an HDS environment that complies with the GDPR.

Carbon Footprint

EcoClin, the carbon footprint calculator for your clinical trials

Developed by CLINACT, the first #GreenCRO, EcoClin is the first carbon footprint calculator designed specifically for clinical trials. It helps sponsors, pharmaceutical companies, and institutions anticipate and optimize the environmental impact of their trials without compromising scientific quality or patient safety.

EcoClin 1st carbon footprint calculator for clinical trials

CARBON FOOTPRINT Calculator designed for clinical trials

Scientific approach: a methodology based on research publications and international task forces.

Scenario simulation: estimating the impact of methodological and logistical choices to determine the most responsible design.

Suitable for all types of studies: applicable to pre- and post-marketing studies for drugs, medical devices, and any health product.

Discover Clinfile, your digital partner in the life sciences

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Regulatory Framework

Compliance & Security

Our services comply with the most stringent regulatory frameworks governing health data.

HDS Hosting

Your clinical data is hosted exclusively by providers certified as Health Data Hosts, in accordance with the requirements of the ANS and the Public Health Code.

GDPR Compliance

Your clinical data is hosted exclusively by providers certified as Health Data Hosts, in accordance with the requirements of the ANS and the Public Health Code.

Our teams are at your service

contact@multihealthgroup.com

01 80 13 14 70

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