Audience
Pharma and biotech companies seeking a solution to improve their visualization of data
About BSI CTMS
BSI CTMS convinces with his trend-setting interface and the intelligent visualization of data. Behind the optics, our clinical trial management software is packed with functions that support pharma, biotech and diagnostics sponsors, as well as CRO and academics (SMO) in their daily world for managing clinical trials in a targeted way. BSI CTMS is being constantly further developed, based on market requirements and in close collaboration with our existing customers. BSI CTMS stands out with its comprehensive functionality, providing CTMS, eTMF, Study Startup and Trial Supply Management RTSM in one integrated unified platform. It’s time to say goodbye to Excel and other stand-alone solutions. You decide if BSI CTMS shall be hosted in the cloud by BSI or on-premise on your IT infrastructure, it is up to you! You can even start in the BSI cloud in order to speed up the project implementation and then later change to on-premise hosting. No vendor locking using BSI CTMS.
Other Popular Alternatives & Related Software
Clinion CTMS
Most Easy-to-Use Clinical Trial Management System (CTMS)
𝐂𝐥𝐢𝐧𝐢𝐨𝐧 𝐂𝐓𝐌𝐒 integrates seamlessly with Clinion EDC and Clinion RTSM to provide detailed and faster access to the entire trial process to address all aspects of Clinical trial management from a single platform: investigator sites, patients enrollment, SAEs, deviations, inclusions, visit scheduling, IP management, milestones, finances, custom reports, and on-demand analytics enables you to improve quality, control risk, and reduce costs.
Our Clinical Trial Management System allows CROs and Sponsors to monitor the trial progress actively with its advanced dashboard and alert notification system. So you’ll never miss a deadline again!
What can you expect?
Comprehensive CTMS Software
Single Source for your entire trial data
On-demand Analytics for Risk-Based Management of Clinical Trials
Fully Integrated with Clinion EDC and Clinion RTSM
100% web-based and hosted securely on the cloud
21 CFR Part 11 & GD
Learn more
Cloudbyz eTMF
Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related documents with a centralized overview. Manage essential trial documents, stay inspection ready, and enable real-time visibility for CROs, sponsors, monitors, and other stakeholders in a clinical trial.
Cloudbyz eTMF is built on the cloud, enabling Sponsors, CROs, and Sites to manage their trial documents with the highest levels of efficiency and integrity. The solution benefits are listed below -
1. Secure, reliable & scalable
2. Compliant & inspection ready
3. Flexible & easy to use
4. Real-time visibility of TMF completeness
5. Collaboration with Site/ Sponsor/CRO
Learn more
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
Learn more
cubeCTMS
cubeCTMS is a comprehensive clinical-trial management system designed to provide end-to-end oversight of trials, from site and investigator tracking, enrollment management and visit scheduling through budget and contract workflows, milestone reporting and document control. It centralizes study operations and automates key processes so sponsors, CROs and study teams can monitor progress in real time, manage tasks across multiple studies, improve site communications and mitigate risk. With built-in dashboards, alerts and audit-ready logging, cubeCTMS supports regulatory compliance (including FDA 21 CFR Part 11 readiness) and enables stakeholders to manage trial timelines, resources and performance from one platform. The system integrates with other CRScube modules (such as EDC, eTMF, pharmacy/RTSM) to provide a unified ecosystem that reduces duplication, improves data flow and supports adaptive workflows during amendments or global roll-outs.
Learn more
Integrations
Company Information
BSI Business Systems Integration AG
Founded: 1996
Switzerland
www.bsi-lifesciences.com/solutions/ctms.html
Videos and Screen Captures
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Product Details
Platforms Supported
Cloud
Training
Documentation
Webinars
Live Online
In Person
Support
Online
Phone Support
24/7 Live Support
BSI CTMS Frequently Asked Questions
BSI CTMS Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Supported
Document Management
Supported
Enrollment Management
Supported
Monitoring
Supported
Recruiting Management
Supported
Scheduling
Supported
Study Planning
Supported
Electronic Data Capture
Not Supported
HIPAA Compliant
Not Supported
Patient Database
Not Supported
