Groupe Multihealth
MultiHealth Group is dedicated to facilitating and accelerating clinical research through innovative solutions, project management, digital tools, qualified talent recruitment, and training. With decades of expertise, the company aims to improve the quality and efficiency of clinical studies while promoting sustainability and environmentally responsible practices in healthcare research.
Industries
Nr. of Employees
medium (51-250)
Groupe Multihealth
Products
Remote monitoring and remote source data verification platform
A digital platform enabling remote source data checks and monitoring workflows to support decentralised monitoring and reduce on-site visits.
Clinical study management platform
Software to manage clinical study operations in real time, integrating study tracking, reporting and operational dashboards.
Clinical trial carbon footprint calculator
A tool to estimate the carbon footprint of clinical trials and select methodologies to measure environmental impact.
Online resource booking portal
Web portal to request and reserve short-duration resources or deliverables for clinical projects, with a 48-hour response target for short requests.
Remote monitoring and remote source data verification platform
A digital platform enabling remote source data checks and monitoring workflows to support decentralised monitoring and reduce on-site visits.
Clinical study management platform
Software to manage clinical study operations in real time, integrating study tracking, reporting and operational dashboards.
Clinical trial carbon footprint calculator
A tool to estimate the carbon footprint of clinical trials and select methodologies to measure environmental impact.
Online resource booking portal
Web portal to request and reserve short-duration resources or deliverables for clinical projects, with a 48-hour response target for short requests.
Services
Clinical trial project management
End-to-end project management for clinical studies including protocol development, study setup, operational coordination and cross-functional oversight for interventional and non-interventional studies.
Outsourced resourcing and rapid staffing (booking portal)
Provision of qualified consultants and short-term operational resources via an online booking portal with rapid request handling for assignments under two months and options for longer engagements.
Digital clinical platform development and implementation
Design and deployment of software solutions for study management and data capture, including CTMS, eTMF, EDC/eCRF, ePRO and remote monitoring integrations.
Biostatistics and data analysis services
Statistical planning, analysis and biometrics support for study design, sample size estimation, data analysis and reporting.
Regulatory documentation, medical writing and pharmacovigilance
Preparation of regulatory documents, medical writing services and safety monitoring for clinical and post-marketing studies, aligned with current GCP and regulatory guidance.
Training academy and webinars
Courses, webinars and live sessions to train clinical research personnel on study design, monitoring, regulatory updates and operational best practices.
Clinical trial project management
End-to-end project management for clinical studies including protocol development, study setup, operational coordination and cross-functional oversight for interventional and non-interventional studies.
Outsourced resourcing and rapid staffing (booking portal)
Provision of qualified consultants and short-term operational resources via an online booking portal with rapid request handling for assignments under two months and options for longer engagements.
Digital clinical platform development and implementation
Design and deployment of software solutions for study management and data capture, including CTMS, eTMF, EDC/eCRF, ePRO and remote monitoring integrations.
Biostatistics and data analysis services
Statistical planning, analysis and biometrics support for study design, sample size estimation, data analysis and reporting.
Regulatory documentation, medical writing and pharmacovigilance
Preparation of regulatory documents, medical writing services and safety monitoring for clinical and post-marketing studies, aligned with current GCP and regulatory guidance.
Training academy and webinars
Courses, webinars and live sessions to train clinical research personnel on study design, monitoring, regulatory updates and operational best practices.
Expertise Areas
- Clinical trial management
- Clinical operations and monitoring (including decentralized trials)
- Digital health platforms for clinical research
- Biostatistics and biometrics
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF)
- Electronic Data Capture (eCRF) and eCRF generator
- Electronic Patient-Reported Outcomes (ePRO)