Products

A leading Clinical Trial Knowledge Platform, offering a transformative collaboration channel and clinical trial oversight.

Electronic Trial Master File for compliant document storage, workflows, and inspection readiness. • Templates, versioning, electronic signatures, and role-based access. • QC workflows and audit trails aligned with GxP and 21 CFR Part 11 requirements.

Clinion eTMF Help teams manage clinical trial documents in a structured way, with real-time tracking and consistent oversight. It reduces the need for manual follow-ups and keeps documentation aligned with study requirements throughout the trial. What can you expect? ● Defined TMF Structure Set up file plans using standard or custom structures across study, country, and site levels. ● Real-Time Tracking of Documents Track expected documents and identify missing or delayed files as the st

Quartz PCI-CFR is a specialized version of Quartz PCI built for laboratories that must manage digital microscope images in compliance with FDA 21 CFR Part 11 regulations governing electronic records and electronic signatures. It is designed for pharmaceutical, biotechnology, and medical device labs where digital images function as regulated records, not just working files. Unlike text documents, where comparing two versions reveals exactly what changed, it is generally not possible to tell what

A new breed of cloud-based, patient-centric data capture solutions designed to handle both ePRO and EDC on BYOD.

Jeeva eClinical cloud helps clinical researchers, patient advocacy groups, clinical research organizations (CROs), public health research organizations, and Biopharmaceutical sponsors to accelerate remote patient recruitment by 3x faster by reducing the logistical burdens on patients and study teams by over 70%. This modular software design allows a rapid study configuration with the features and workflows that fit the specific trial protocol whether short-term or long-term, cross-sectional or

Velos eResearch connects financial, administrative and clinical research activities, you can do away with the patchwork of manual and partially automated systems common in clinical research today.

ThoughtSphere’s mission is to help life science companies develop and deliver treatments to patients faster and smarter using data science. With our innovative platform, biopharma, medical device sponsors and CROs not only can reduce and optimize clinical development costs but also enhance efficiency and effectiveness in the clinical trial processes, and gain near real-time actionable insights. Founded by clinical information and technology industry experts, ThoughtSphere aims to deliver on the

LifeSphere is an end-to-end life sciences platform, using ArisGlobal’s proprietary Nava® cognitive computing engine to automate all core functions of the drug development process. Offering simple integration with our next-generation LifeSphere EasyDocs document management solution across the product lifecycle, the LifeSphere platform helps life sciences companies reduce time to market, increase compliance and lower drug development costs.