ResearchManager

What is ResearchManager?

The ResearchManager Clinical Research Suite offers a comprehensive set of digital tools to streamline clinical data management and clinical operations, empowering organizations to efficiently conduct qualitative and efficient clinical research. This modular eClinical platform provides Electronic Data Capture (EDC), Electronic Patient Reported Outcomes (ePRO), Randomization and Trial Supply Management (RTSM), and Electronic informed consent (eConsent) for clinical data management, as well as Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), Laboratory Information Management System (LIMS), and Regulatory Information Management System (RIMS) for clinical operations. With over 10 years of experience, 20,000+ active users, and 25,000+ global studies conducted, ResearchManager is a validated partner for CROs, Pharma, Biotech, MedTech, Academic institutions, Healthcare providers, and Medical Ethical Committees/Institutional Review Boards (IRBs) entities, offering compliance with standards such as 21 CFR Part 11, HIPAA, GCP, GDPR, and ISO 14155

Highlights

• Electronic Data Capture (EDC) for collecting, validating, and enriching clinical data
• Electronic Patient Reported Outcomes (ePRO) for collecting digital patient data during hybrid or decentralized clinical trials
• Randomization and Trial Supply Management (RTSM) for streamlining randomization, stratification, and inventory management processes
• Electronic informed consent (eConsent) for digitally screening and consenting participants during hybrid and decentralized clinical trials
• Clinical Trial Management System (CTMS) for effectively managing and tracking the entire study start-up and portfolio
• Electronic Trial Master File (eTMF) for centrally storing and organizing documentation, expediting signatures, and optimizing site management
• Laboratory Information Management System (LIMS) for managing laboratory and biobank activities, including sample registration and data management
• Regulatory Information Management System (RIMS) for supporting Regulatory Affairs teams, Ethics Committees, Sponsors, CROs, and other stakeholders in managing essential documentation