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Research sarjen@sarjen.com Clinical Trial Management Software – CTMS Research sarjen@sarjen.com Home Solutions Smart Trial Suite – Early Phase Smart Trial Suite – Late Phase Smart Trial Suite – Oncology Trials Smart Trial Suite – Registry Trials Post Approval Trials Bioanalytical Laboratory Automation Services Implementation Models Trial suite qualification Randomization and Investigational Product Supply Management as a Service Competencies Project Management Clinical Research Biometric Volunteer Registration Medical Screening Protocol Training and Duty Delegation Randomization and Investigational Product Supply Management Electronic Case Record Form (eCRF) Electronic Data Capture (EDC) Clinical Data Management (CDM) Electronic Patient Reported Outcome (ePRO) Clinical Laboratory Management Patient Compensation CT Tracker Sample Inventory Management Bioanalytical Laboratory Automation Diagnostic Imaging Software (DI Soft) CDISC SDTM Electronic Trial Master File (eTMF) Resources Blogs Case Studies Webinars White PapersContact us Top Menu Home Solutions Smart Trial Suite – Early Phase Smart Trial Suite – Late Phase Smart Trial Suite – Oncology Trials Smart Trial Suite – Registry Trials Post Approval Trials Bioanalytical Laboratory Automation Services Implementation Models Trial suite qualification Randomization and Investigational Product Supply Management as a Service Competencies Project Management Clinical Research Biometric Volunteer Registration Medical Screening Protocol Training and Duty Delegation Randomization and Investigational Product Supply Management Electronic Case Record Form (eCRF) Electronic Data Capture (EDC) Clinical Data Management (CDM) Electronic Patient Reported Outcome (ePRO) Clinical Laboratory Management Patient Compensation CT Tracker Sample Inventory Management Bioanalytical Laboratory Automation Diagnostic Imaging Software (DI Soft) CDISC SDTM Electronic Trial Master File (eTMF) Resources Blogs Case Studies Webinars White PapersContact us BizNET – a Comprehensive suite of solutions for Clinical Research Automated entire trial life cycle Manage and Track complete study/trial aspects Integrated Platform for Phase I – IV trials CDISC SDTM - New curve in eClinical Data Integrity Integrated with standardized library of domain models and their attributes Easy to design/Reuse and implement templates for study, protocols Clinical data mapped with CDISC SDTM standards Electronic Data Capture and Record Management Easy reporting, easy archival Volunteer-/Patient- wise electronic data capture Generate, manage, clean and validate clinical data with audit trails Data export to EXCEL, PDF or SAS (for statistics) Study setup and eCRF designing In-built template repository for reuse Allows to enter validation checks Intuitive and easy CRF designing Maintain document versions, adhere to CDISC standards User friendly and, also, available on Cloud Unique features that best supports Clinical processes Immensely secure, low maintenance Easy to understand and access Smart Trial Suite – Early Phase An integrated and comprehensive suite of solutions for early phase and BA-BE trials Read More » Smart Trial Suite – Late Phase A multi-site clinical trial suite of solutions for late phase trials Read More » Smart Trial Suite – Oncology Trials A specifically designed and well-integrated suite of solutions to conduct seamless Oncology Trials Read More » Smart Trial Suite – Registry Trials Suite of solutions to conduct Registry Trials Read More » Smart Trial Suite – Post Approval Trials Suite of solutions to conduct Post approval Trials Read More » BioLyte Suite of solutions for flawless integrated Bioanalytical laboratory automation Read More » BizNET-CTM, a platform for Clinical Research Consists of clinical trials management solution suites for various CROs, Pharmaceutical, Biotech and Medical device industries. BizNET-CTM, is a multi-functional platform which allows a CRO (Contract Research Organization) in planning, managing, designing, executing, monitoring and analyzing trial related activities and data in adherence to the protocol obligations and regulatory requirements. An end-to-end solution suite which cater to the needs of clinical research project starting from Project Management, feasibility assessment, volunteer or patient enrolment using iris recognition technology, capture clinical trial data, multi-level review process, data compilation to data archiving. The BizNET-CTM suite is designed to manage all of the documents, tasks, processes, relationships, audits, and training that must be administered and controlled throughout the life of a clinical trial. The BizNET-CTM Suite is a complete clinical trial management software system designed to streamline and increase reuse of information while simplifying the processes and tasks that need to be executed during the lifespan of a clinical trial. It provides research professionals with faster access to real-time data , allowing them to track and manage their studies from start to finish as well giving the Tracking of the Project on Every Step. The platform features solutions that cover the entire study – from start up to submission. You can gather, organize, analyze and report data for any type, size or phase of trial. BizNET-CTM is a validated software, compliant with Part 11 (21 CFR part 11 and Annex 11), GCP guidelines that involves transparent and smooth process – portraying a clear representation to regulatory bodies and sponsors. Regulatory compliant, multi-functional Clinical trials management software solution for CROs Download Brochure Copyright © 2024 Sarjen Systems Pvt. Ltd. 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