BizNET-CTM - 2026 Pricing, Features, Reviews & Alternatives

BizNET-CTM is a comprehensive clinical trial management software platform designed for Contract Research Organizations, pharmaceutical, biotech, and medical device industries. The multi-functional platform enables research professionals to plan, manage, design, execute, monitor, and analyze trial-related activities while ensuring adherence to protocol obligations and regulatory requirements. The system supports various clinical research scenarios including early phase, late phase, oncology trials, registry trials, and post-approval trials, providing specialized functionality for each trial type while maintaining a cohesive workflow environment for organizations managing diverse clinical studies.

The platform features integrated capabilities covering the entire clinical trial lifecycle, from project management and feasibility assessment to data archiving. Core functionalities include volunteer or patient enrollment with iris recognition technology, electronic data capture, electronic case record form management with template repositories, multi-level review processes, and comprehensive data compilation. BizNET-CTM incorporates specialized modules for biometric volunteer registration, medical screening, protocol training, randomization, investigational product supply management, clinical data management, electronic patient reported outcomes, laboratory management, patient compensation tracking, sample inventory management, and diagnostic imaging.

The system integrates CDISC SDTM standards with library domain models, enabling consistent data mapping and improved data integrity throughout the research process.BizNET-CTM operates as a validated software solution compliant with 21 CFR Part 11, Annex 11, and Good Clinical Practice guidelines. The platform facilitates data export to Excel, PDF, or SAS formats for statistical analysis and provides integration with bioanalytical laboratory automation through its BioLyte module. Its electronic trial master file functionality ensures proper documentation management throughout the trial process.

Available in both traditional and cloud-based deployment models, the system offers organizations implementation flexibility while maintaining security standards and minimal maintenance requirements. The architecture supports transparent processes that provide clear representation to regulatory bodies and sponsors, making it valuable for organizations managing complex clinical trials requiring rigorous documentation and regulatory compliance.