by Meditrial
Electronic data capture and clinical trial data management with instant validation and real-time access for global studies.
Clinical Trial Managementby Meditrial
Patient-reported outcomes, electronic consent, and clinical outcome assessment for real-time, compliant data collection in clinical trials.
Clinical Trial Managementby Meditrial
Certified training courses on medical device regulation, clinical trials, and product standards.
Commercial & Medical Affairs
by Certivo
FDA 21 CFR Part 11 compliant electronic signatures with ALCOA+ audit trails and 25-year retention for clinical trials and regulated life sciences.
Quality, Compliance & Regulatory
by InfoEd Global
Clinical trial design, enrollment tracking, document management, and financial administration for research institutions.
Clinical Trial Managementby InfoEd Global
IRB, IACUC, environmental safety, and conflict of interest management for research compliance and ethics oversight.
Quality, Compliance & Regulatoryby InfoEd Global
Real-time inventory, ordering, and location tracking for animal research facilities throughout the research lifecycle.
Lab Informatics & Operationsby InfoEd Global
Collect, manage, and report research publications and outputs to quantify performance, ensure compliance, and support institutional funding goals.
Lab Informatics & Operations
by Clinevo Technologies
End-to-end pharmacovigilance with case intake, processing, regulatory submissions, and signal detection in a unified system.
Regulatory & Safety Documentationby Clinevo Technologies
AI-driven case processing, regulatory submissions, and safety signal detection for pharmacovigilance workflows.
Regulatory & Safety Documentationby Clinevo Technologies
Adverse event and medical inquiry intake from MICC, email, web, and forms with real-time tracking and regulatory compliance.
Regulatory & Safety Documentationby Clinevo Technologies
Automated signal detection and management for pharmacovigilance with quantitative algorithms, smart triaging, and regulatory compliance.
Regulatory & Safety Documentationby Clinevo Technologies
Automated literature search and retrieval from PubMed, EMBASE, and journals with seamless pharmacovigilance database integration.
Regulatory & Safety Documentationby Clinevo Technologies
Electronic management of Safety Data Exchange Agreements and Pharmacovigilance Agreements with automated workflows, version control, and compliance tracking.
Regulatory & Safety Documentationby Clinevo Technologies
End-to-end clinical trial management with CTMS, EDC, eCOA, eConsent, and remote monitoring for decentralized and hybrid trials.
Clinical Trial Managementby Clinevo Technologies
Document organization, tracking, and compliance management for clinical trials with DIA-compliant structure and 21 CFR Part 11 audit trails.
Clinical Trial Managementby Clinevo Technologies
Capture, validate, and manage clinical safety data with integrated medical coding, real-time monitoring, and regulatory compliance for pharmacovigilance workflows.
Clinical Trial Managementby Clinevo Technologies
Patient, caregiver, and clinician outcome data capture for decentralized and hybrid clinical trials. 21 CFR Part 11 compliant.
Clinical Trial Managementby Clinevo Technologies
Electronic consent and case processing for clinical trials with multimedia support, real-time compliance monitoring, and decentralized study capabilities.
Clinical Trial Management
by Folio3
AI-powered medical imaging analysis and report generation with DICOM viewing, secure sharing, and Epic EHR integration.
Digital Pathology & Imaging