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Highly rated by customers | 
4.2 / 5 stars
The all-in-one platform for smarter and faster clinical research at every stage
Every day, patients wait for treatments that are still in development. To speed up the path to new treatments, the Clinical Research Suite helps CROs, sponsors, universities, and hospitals streamline operational processes and data collection at every stage of the research process.
Trusted by over 200 organizations
A modular suite that adapts to your situation
Every clinical trial is unique in its phase, design, and methodology, requiring support tailored to its specific needs. The Clinical Research Suite offers a modular structure with flexible tools that can be used individually or combined, depending on the study requirements. When customization is needed, our consultants configure the tools to align with the study protocol and team workflow.
Study Design & Approval
Stay on top of study processes and documentation
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CTMS: Manage and monitor your clinical study from start to finish by centralizing operational processes in one comprehensive environment. -
eTMF: Keep your Trial Master File organized at all times with centralized document storage, version control, role-based access, and eISF for multicenter studies.
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RIMS: Streamline regulatory and ethics approvals by centralizing documentation, communication, and submission tracking.
Recruitment & Participation
Recruit and include the right participants
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Patient Recruitment: Reach the right participants faster with QR codes and web links, direct screening, and real-time enrollment tracking.
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eConsent: Simplify the consent process with customizable templates, legally valid e-signatures, and automatic archiving of informed consent forms.
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Visit Planning: Prevent missed or incorrectly scheduled appointments by organizing patient visits by treatment, healthcare provider, and location.
Data Collection
Easily collect data, both on-site and decentralized
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EDC: Record patient data accurately with real-time validation and immediate insight into study data.
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RTSM: Reliably randomize participants based on stratification factors, with automatic synchronization of assignment and inventory.
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ePRO: Increase participant engagement with accessible questionnaires that participants can complete at any time, on any device, and from any location.
Built for compliant clinical research
Success Stories from Our Users
For more than 13 years, CROs, sponsors, universities, and healthcare institutions have relied on the Clinical Research Suite to conduct structured and reliable clinical research. Read how other organizations have successfully improved their research processes using smart digital tools.
Why ResearchManager?
Always compliant
Our software is fully compliant with all relevant laws and regulations. If the regulations change, we will update the software at no cost.
Proven to be faster
Organizations work more efficiently and achieve validation faster with the Clinical Research Suite. If that doesn’t work, our consultants will fix it at no cost.
Our users have expressed their appreciation
Thanks to independent, verified user reviews on G2, our platform has received several badges. Users have given positive feedback on ease of use, support, implementation, and ROI. The badges demonstrate that our platform is not only actively used but also highly valued.
G2 Momentum Grid – CTMS/eTMF
Hans Middelweerd
Global Sales Manager - Academic & Healthcare
Thierry Wetting
Global Sales Manager - CROs & Sponsors
