Comprehensive Clinical Trial Management Software
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Complete workflow automation for Clinical Site : Protocol driven Clinical trial management system
Automatic eCRF generation for In-study and Post study : 21 CFR Part 11 and GCP Compliant Software System
Secured web based remote monitoring : Effective management of multiple simultaneous studies
Alerts and Adverse Events Management : Data Security and Integrity
We are offering comprehensive clinical trial management software. bioclinical, a 21cfr part 11 compliant electronic data capture tool that automates the workflow of clinical trials/sites. the sound knowledge of it, analytical instrumentation, clinical and pharmaceutical domain and regulatory compliances has helped bio-analytical technologies®(b.a.t.) to develop this solution using latest tools and technology. Bioclinical enhances the overall productivity by automating most of the current manual operations like: -- subject registration -- protocol creation and approval -- subject selection for screening and study -- crf in study activities -- adverse events and deviation handling -- crf post study -- sample management -- investigational product management -- generation of following report: protocol, protocol synopsis, screening, lab test, crf in study, protocol deviation, adverse event and clinical study report. Bioclinical fulfills the important requirements like subject management, compliance with government regulations, and compatibility with other data management systems.
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We are offering document management system. Document management system is a computer system (or set of computer programs) used to track and store electronic documents.
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