Clinical Trial System

UK hospitals

Healthcare organizations, including hospitals in the United Kingdom, mental health care institutions, and private healthcare providers, deliver high-quality care to patients. Clinical research is a part of this process. It is crucial for these institutions to have effective tools to optimize clinical research, manage data accurately, and comply with strict laws and regulations. ResearchManager offers healthcare organizations a comprehensive range of tools to support them in improving their clinical and operational efficiency, tailored to the specific needs of the healthcare sector. Our tools are indispensable for innovation in patient care and streamlining the clinical research process. Explore the setups and possibilities.

Improved Processes and Document Management with CTMS and eTMF

In healthcare organizations, various units such as the medical staff, research offices, and administrative departments work closely together to provide high-quality care. ResearchManager CTMS and eTMF are integrated tools that support healthcare organizations in their clinical research processes, including efficient coordination and documentation management.

Reliable Data Collection with EDC

In healthcare organizations, accurately capturing clinical data is crucial for making diagnoses and determining appropriate treatment plans. ResearchManager provides an advanced Electronic Data Capture (EDC) system that supports healthcare providers in efficiently and accurately collecting, managing, and analyzing clinical research data. Patient care improves through faster decision-making based on reliable information.

Improved Patient Data with ePRO and eConsent

With ePRO (Electronic Patient-Reported Outcomes), patients can easily capture data about their health and well-being, resulting in a better understanding of their overall health status. By having patients complete questionnaires, the patient-reported outcomes are integrated into the research results. With ePro, we simplify the collection of this data, leading to time savings and improved data quality.

Simultaneously, eConsent streamlines the process of obtaining consent for participation in clinical research, resulting in smooth participant recruitment and increased engagement, while healthcare organizations simultaneously comply with regulations. This strengthens the relationship between healthcare providers and patients, ultimately enhancing the quality of care.

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