BSI CTMS

The BSI CTMS is a Clinical Trial Management System designed for optimal efficiency and usability in managing modern clinical trials. It features a user-optimized interface with smart data visualization capabilities.

Benefitting sectors such as pharma, biotech, diagnostics, med-tech sponsors, contract research organizations (CROs), and academic bodies, the CTMS facilitates daily trial management, continually evolving through input from market demands and existing customer feedback.

Key Benefits of BSI CTMS:

• Comprehensive Functionality: This system covers all clinical trial stages, from initiation to closure, and supports both interventional and non-interventional studies across all scales.
• User-Friendliness: With a modern HTML5 web interface, it is noted for ease of use, aiding in making daily tasks more efficient and enjoyable.
• Seamless Integration: The system easily integrates with various other clinical systems through standard interfaces, supporting single-sign-on and more.
• Cost Efficiency: Offers low total cost of ownership due to minimal training needs and vendor-independent upgrades included in licensing.
• Robust Reporting: Provides flexible reporting features, allowing customizable or pre-configured reports exportable to Word, Excel, and PowerPoint.
• Regulatory Compliance: Ensures adherence to global regulations like 21 CFR Part 11 and GDPR, with regular updates for continued compliance.
• Comprehensive CRO Modules: Includes features for business development, contract management, invoicing, and HR management, functioning as an ERP system for CROs.

The BSI CTMS unifies functionalities such as CTMS, electronic Trial Master File (eTMF), Study Startup, and Trial Supply Management on a single platform, enabling organizations to transition away from fragmented, Excel-based systems.