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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. 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 technological approach enhances the efficiency, traceability, and security of your studies, while complying with ICH-GCP, CDISC, and 21 CFR Part 11 guidelines.

High-Performance EDC and CTMS Solutions

Certified EDC platforms: secure electronic data collection tools hosted in an HDS environment.

CTMS: Clinical Trial Management Systems for centralized project management.

Custom integration: configuring tools according to the specific requirements of each protocol.

Distantia, our remote monitoring platform

Monitoring: A 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.

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.

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

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

Clinfile

Compliance & Security

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

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

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