Versatile and Robust clinical trial management solutions for Biopharmaceuticals, Contract Research Organization (CRO), Life Sciences and Medical device manufacturing companies of all sizes.

BizNET-CTM (BizNET – Clinical Trial Management) is a comprehensive clinical trial management software developed by Sarjen.

BizNET-CTM is a fully validated, 21 CFR Part 11 and GCP compliant clinical trials management software solution which cater to complete the life cycle of BA/BE and clinical trial studies.

BizNET-CTM provides modules for managing, planning, designing, monitoring, tracking and archiving the trial related activities and investigator information on a centralized database. We have been providing end-to-end Direct Data Capture & eClinical Technology solutions.

Its flexibility and user friendliness make the management of clinical trials faster and easier. Its capabilities assist in producing the validated results which are accurate, accessible and reproducible with full complete audit trail facility.

BizNET-CTM electronic software not only save the cost of paper but also make entire clinical trial process smooth and transparent to regulatory authorities. The dynamic multi-level review process maintains the accuracy and integrity of the data generated.

BizNET Clinical Trial Management also allows an organization to have multi-disciplinary approach in project management for pro-active decision making and collaboration with the global clinical research organization. Better user interfaces meeting the highest requirement for usability from ground to final level. The final outputs from the system is designed and developed to suit the requirement of the statistical department and further studies. System helps to maintain the updated data with the help of high performance real time data synchronization mechanisms.

Salient Features:

Web based solutions

Enhanced patient recruitment management using Iris recognition technology

Actualize end-to-end trial processes

Intuitive eCRF designing tools

Can be used for multi-center CRO and multi-site study

Customized reports and Dashboard

Data Management

Data Archival

Medical Coding

Data export to PDF, EXCEL, CDISC and SAS formats

Track drug kits, supplies, AEs/SAEs, and more

Discrepancy management

Edit-check execution reports

Online Site Monitoring

Online data transcription

Single platform to track status, visits and site progress

Highlights:

21 CFR part 11 and GCP compliant

Audit trail in entire process

Multi-level Data Review process

Electronic signature & records

Data security and Integrity

Secured data transfer terminal from client to server

Instant validation

Regulatory compliant, multi-functional Clinical trials management software solution for CROs

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