Discover Our New CTMS
Audit Module for Sponsor Oversight
Mobile CRA Reconciliation, eTMF Document Capture and Processing, and Content Collaboration
Document Auto-Naming and Auto-Routing
Predictive Insights
Configurable KPIs
Configurable Dashboards and Reporting
Powerful Document Search
Trial Correspondence/Email Capture
Query Management
Flexible and Configurable to Requirements
Expedites Site Activation and Document Work Streams
Comprehensive, Easy-to-Use Workflows
Mobile eTMF, CRA Reconciliation, and Document Collaboration
Fast Implementation and User Onboarding/Adoption
21 CFR Part 11, Annex 11, ERES, GxP/GCP, GAMP 5, and GDPR Compliant
Understanding the Scope and Pain Points of Study Start-Up - Part 2
In this series of webinars, experts will highlight the difficulties behind Study Start-Up and provide you some solutions to those pain points along the way.
Reducing IT Burden on Small and Mid-Sized Pharma & Biotechs
In this webinar, our Head of Product, Jay Smith, discusses the ways in which a complete and connected eClinical platform can help reduce the IT burden for small to mid-sized pharma and biotechs.
Trial Interactive Ask and Expert: The TMF Reference Model
In this Ask an Expert webinar, Gillian Gittens, our director of eClinical Strategy and Solutions, answers your TMF Reference Model questions.