Clinact
MultiHealth Group is a leading provider in clinical research, offering a comprehensive range of services including project management, outsourcing, digital solutions, and training. With decades of expertise, the company is committed to facilitating and accelerating clinical research through innovative, sustainable practices and digital tools, aiming to improve healthcare and patient outcomes globally.
Industries
Nr. of Employees
medium (51-250)
Clinact
Products
Remote monitoring / source data control platform
A digital platform enabling remote source data control and monitoring workflows to check data quality collected during clinical trials and reduce on-site visits.
Clinical study management platform (CTMS/eTMF/eCRF/ePRO)
Secure, real-time digital solution to optimise management, monitoring and analysis of clinical studies, incorporating CTMS, eTMF, eCRF and ePRO capabilities.
Clinical trial carbon footprint calculator
Tool to select a methodology and calculate the carbon footprint of a clinical trial to assess environmental impact of study decisions.
Resource and deliverable booking portal
Online form and portal to request short-term resources or deliverables (under two months) with rapid processing and assignment.
Remote monitoring / source data control platform
A digital platform enabling remote source data control and monitoring workflows to check data quality collected during clinical trials and reduce on-site visits.
Clinical study management platform (CTMS/eTMF/eCRF/ePRO)
Secure, real-time digital solution to optimise management, monitoring and analysis of clinical studies, incorporating CTMS, eTMF, eCRF and ePRO capabilities.
Clinical trial carbon footprint calculator
Tool to select a methodology and calculate the carbon footprint of a clinical trial to assess environmental impact of study decisions.
Resource and deliverable booking portal
Online form and portal to request short-term resources or deliverables (under two months) with rapid processing and assignment.
Services
End-to-end operational support for clinical trials from protocol design through implementation and close-out, including clinical operations, biometrics and regulatory operations.
Provision of qualified consultants and short-term deliverables with rapid processing of requests (booking portal and resource matching within 48 hours for short assignments).
Design, development and deployment of secure platforms for trial management and data capture, including CTMS, eTMF, eCRF/ePRO systems and remote monitoring tools.
Statistical planning and analysis, biometrics, database management and reporting for clinical trials and observational studies.
Safety monitoring for clinical and post-marketing phases and production of regulatory, clinical and scientific documentation.
Practical and theory-led training programmes and webinars delivered by clinical research experts to build competency in study design, operations and analytics.
End-to-end operational support for clinical trials from protocol design through implementation and close-out, including clinical operations, biometrics and regulatory operations.
Provision of qualified consultants and short-term deliverables with rapid processing of requests (booking portal and resource matching within 48 hours for short assignments).
Design, development and deployment of secure platforms for trial management and data capture, including CTMS, eTMF, eCRF/ePRO systems and remote monitoring tools.
Statistical planning and analysis, biometrics, database management and reporting for clinical trials and observational studies.
Safety monitoring for clinical and post-marketing phases and production of regulatory, clinical and scientific documentation.
Practical and theory-led training programmes and webinars delivered by clinical research experts to build competency in study design, operations and analytics.
Expertise Areas
- Clinical trial management
- Study design and adaptive trial methodologies
- Digital health and clinical trial IT
- Biostatistics and data management
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF)
- Electronic Case Report Form (eCRF) and eCRF generator
- Electronic Patient-Reported Outcomes (ePRO)
News & Updates
The MultiHealth Group will once again be present at this key event for innovation in healthcare in Europe with FORMATIS.
At this event organised by APEC, FORMATIS and TempoPHARMA will once again be on hand to discuss the careers of tomorrow.
The design of a clinical study corresponds to the methodology chosen to conduct a clinical study to answer a defined medical research question.
Biostatistics plays a crucial role in human health studies, transforming raw data into meaningful information to facilitate informed decision-making.
Good clinical practice is evolving to meet today’s challenges. ICH E6 R3 introduces key innovations designed to enhance the quality, transparency and ethics of clinical trials.
The MultiHealth Group will once again be present at this key event for innovation in healthcare in Europe with FORMATIS.
At this event organised by APEC, FORMATIS and TempoPHARMA will once again be on hand to discuss the careers of tomorrow.
The design of a clinical study corresponds to the methodology chosen to conduct a clinical study to answer a defined medical research question.
Biostatistics plays a crucial role in human health studies, transforming raw data into meaningful information to facilitate informed decision-making.
Good clinical practice is evolving to meet today’s challenges. ICH E6 R3 introduces key innovations designed to enhance the quality, transparency and ethics of clinical trials.