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Regulatory Information Management System (RIMS) is widely used in the clinical research sector by various stakeholders, including Contract Research Organizations (CROs), Institutional Review Boards (IRBs), Ethical Committees (ECs), biotechnology companies, pharmaceutical organizations, and academic research institutions. These systems are an integral part of managing regulatory documentation and help streamline processes to comply with regulatory standards in clinical research.

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The Regulatory Information Management System (RIMS) is essential in clinical trials to comply with strict regulatory standards. The system provides streamlined storage, management, and reporting of all regulatory documents required for clinical trials. This includes managing protocols, research reports, approvals, and other necessary documentation for regulatory compliance and audits.

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ResearchManager LIMS automates and manages laboratory processes, making it more efficient to track samples, conduct tests, and analyze data. This leads to better laboratory management, increased accuracy, improved data integrity, and timely reporting of results.

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Yes, there is integration between Clinical Trial Management Systems (CTMS) and electronic Trial Master Files (eTMF). This integration streamlines the exchange of data and documents between systems, enhancing the management of essential documentation and regulatory requirements for clinical research.

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ResearchManager eTMF, a tool within the Clinical Research Suite (CRS), automates the management of trial master files, making it easy for research teams to store, organize, track, and validate documents. The system promotes compliance through centralized, organized, and secure storage of essential documents, supporting inspection and audit preparation while readying the Investigator Site File (ISF). It also includes an integrated and validated eSign module for immediate signatures.

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ResearchManager CTMS is highly adaptable, allowing customers to tailor functionalities to their specific needs. This includes the ability to customize reports, create customized dashboards, and configure workflows, enabling research teams to create a tailored solution that meets their unique requirements.

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ResearchManager CTMS enhances operational efficiency by offering comprehensive functionalities such as managing workflows, approval processes, report generation, communication, and more. These features optimize project planning, resource management, and patient monitoring, increasing the operational pace and overall efficiency of clinical research.

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ResearchManager RTSM, a tool within the Clinical Research Suite (CRS), is suitable for Randomized Controlled Trials (RCTs). RTSM encompasses powerful tools for randomization and inventory management. This feature simplifies the complexity of the inventory chain in clinical research and ensures strict adherence to protocols. Accurately delivering treatments contributes to the safety and integrity of the studies.

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ResearchManager eConsent, a tool within the Clinical Research Suite (CRS), focuses on enhancing participants’ experience by providing them with interactive and understandable information about the research and consent procedures. This makes it easier for participants to engage in studies by providing clear and transparent consent, resulting in better participant engagement and an efficient consent process, whether on-site or remotely via the web, phone, or tablet.

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ResearchManager ePRO, a tool within the Clinical Research Suite (CRS), enables patients to input research data from any location, whether through web, phone, or tablet. This enhances patient participation willingness and maximizes the quality of data recording by providing flexibility in collecting the right data at the right time, supported by schedules for automated data collection.