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    Comprehensive Clinical Trial Management Software

    • Automatic eCRF generation for In-study and Post study21 CFR Part 11 and GCP Compliant Software System
    • Complete workflow automation for Clinical SiteProtocol driven Clinical trial management system
    • Alerts and Adverse Events ManagementData Security and Integrity
    • Secured web based remote monitoringEffective management of multiple simultaneous studies
    • Supply TypeSupplier, Retailer
    • Preferred Buyer Location India only

    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....
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    Company Information

    • calendar Member Since 14 Years
    • building Nature of Business Retailer
    • Year of Establishment 2003

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    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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