MultiHealth Group

International, Mises en place, visites de suivi, contrôle qualité des données

Real-time remote collection, consultation, and monitoring of source data for clinical trials.

Management and tracking services for early access and compassionate use programs (AAC and AAC nominatif) ensuring operational responsiveness and strict regulatory compliance.

CTMS and eTMF providing a consolidated, dynamic view of the progress of each clinical study.

Provide an effective digital response to the need to verify the quality of data collected during your clinical trials through remote source data verification.

Digitization of participant consent and electronic collection of patient-reported outcomes.

Create, store and track all essential documents for a clinical study securely and efficiently.

Innovative solutions to optimize the management, monitoring and analysis of your clinical studies with efficiency and compliance.

Clinfile develops digital solutions for clinical trial management, including secure, intuitive platforms to facilitate data collection, tracking, and analysis.

Outils de collecte électronique des données, sécurisés et hébergés en environnement HDS.

Collect and centralize clinical data from your studies with robust electronic case report form and electronic data capture systems.

Consultants who are experienced in their field and quickly available to meet your needs.

Software for simplifying and securing the management of Early and Compassionate Access programs.

Systèmes de gestion des essais cliniques pour un pilotage centralisé des projets.

Respond to patients' unmet needs by making innovative treatments available to them before they receive market authorization.

Comprehensive clinical project management services covering interventional clinical trials from phases I to IV, multi-stakeholder coordination, and rigorous tracking of timelines, budgets, and quality requirements.

Multidisciplinary teams to ensure coordination, compliance and excellence in the development of your healthcare innovations.

Clinact is a CRO for clinical project management, offering tailor-made support for clinical trials ranging from trial design to implementation.

Statistical expertise and clinical data management services for industrial and academic sponsors supporting clinical studies.

Formations professionnelles pour les metiers de la recherche clinique et epidemiologique proposees par l'organisme FORMATIS du groupe MultiHealth.

FORMATIS offers tailor-made training programs in clinical research delivered by experts to support the development of talent.

Outsourcing and recruitment of qualified resources providing consultants who are experts in clinical and preclinical studies available at short notice.

ECRF, Data Management, Biostatistiques

Services de gestion rigoureuse et réactive des événements indésirables pour les essais cliniques et le suivi post-commercialisation de produits de santé.

Complete, secure record of all actions carried out in any of the systems used for your clinical studies.

Training courses organized by clinical research experts to help you improve your skills or learn a new trade.

Audits, SMQ, ISO 9001, qualité produit

Soumissions, stratégie réglementaire, dossiers d’AMM

Méthodologie, protocole, articles, posters, BI, PSUR, CER, CSR, revue bibliographique

An online booking platform created by MultiHealth Group that enables public and private healthcare companies to book short-term clinical research outsourcing requirements and deliverables under 2 months.

Real World Evidence (RWE) study design and management combined with dedicated expertise in utilizing the French National Health Data System (SNDS) for observational studies and patient pathway modeling.

Specialized statistical analysis and data management services for clinical trials providing scientific rigor and tailor-made solutions.