Audience
A modern web application combining capabilities of database software used in clinical research
About Phoenix CTMS
Phoenix CTMS is a modern web application combining the capabilities of database software used in clinical research in one modular system. After years of collaborative development with trial sites at the Medical University of Graz, the Phoenix CTMS now becomes publicly available (LGPL 2.1). This unmatched feature set is geared to support all operational and regulatory requirements of the clinical front end in academic research, at CROs (Contract Research Organisations) and hospitals conducting clinical studies of any phase. want a CDMS that gives you unlimited Javascript form scripting support (server- and browserside). You need to deal with large eCRFs (electronic case report forms)
want to try a serious open source alternative for eCRFs. Need to formulate complex ad-hoc database queries to list matching subject candidates using set operations. Conduct several trials in parallel and need to organize site staff and resources. Need a software to implement various processes for ICH GCP.
Pricing
Starting Price:
$1 one-time payment
Free Version:
Free Version available.
Integrations
No integrations listed.
Company Information
Medical University of Graz
Austria
www.phoenixctms.org
Videos and Screen Captures
QMENTA
Globally accessible, infinitely scalable, AI-powered, collaborative cloud platform meeting the highest standards of security and compliance. An industry-leading and simple-to-use software platform, purpose-built by neuroimaging and data science experts to meet the distinct and challenging needs of the neuroscience community. Optimized and tailored for your needs, whether you are conducting research, running clinical trials, at the point of care, developing novel algorithms or leveraging brain-related data. Global data aggregation, and consolidation of imaging-based studies in one cloud platform. Streamlined, end-to-end clinical, real-world data and medical imaging data management. End-to-end expert and personalized support to ensure your study success. Centralized reading and the ability to compare quantitative results to a normative database. Highest quality, shareable reporting and data exporting for submissions approval.
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Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM).
Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services.
Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.
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ClinVigilant
Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our:
♦ Fast EDC set-up (less than 4 weeks).
♦ Cost-effectiveness.
♦ 3rd party integrations (including legacy systems).
Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA.
The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem.
How simple and user-friendly is it? Ask for a demo to find out!
Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials.
Enquiries > bd (at) clinvigilant.com
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QuesGen Platform
From simple turnkey solutions to large-scale multi-site studies, we help PIs overcome common obstacles and limitations with their database setup and selection. Researchers also hire QuesGen to advise on data management best practices and provide additional services where needed to help studies get up and running more quickly. Experienced partner for dozens of academic institutions and researchers. Experienced in managing large data sets and running data curation through our flexible data platform. The ability to set up and scale research initiatives quickly and easily. With a comprehensive data model, assessments library, and curation expertise, QuesGen gets you up and running quickly, and ensures quality, compliant data, so you can focus on the analysis of the results. Support multiple clinical research initiatives across your institution using HIPAA and FDA 21 CFR Part 11 compliant solutions that can integrate with your EMR, FITBIR (Federal Interagency TBI Repository.
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Product Details
Platforms Supported
SaaS
Windows
Training
Documentation
Support
24/7 Live Support
Online
Not Offered
Phoenix CTMS Frequently Asked Questions
Phoenix CTMS Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning