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BizNET

Sarjen Systems offers a trio of specialized, GxP-compliant solutions designed to manage the full spectrum of clinical development and laboratory operations. The first is the Early Phase CTMS (BizNET), an end-to-end software suite tailored for early-phase clinical trials and...

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  • Pay once or Subscription
  • Proprietary

Platforms

  • Online
  • Software as a Service (SaaS)
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  • clinical-trials

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BizNET information

  • Licensing

    Proprietary and Commercial product.
  • Pricing

    One time purchase ranging between $200 and $10000, and / or subscription ranging between $500 and $8000 per month.
  • Alternatives

    14 alternatives listed
  • Supported Languages

    • English
BizNET was added to AlternativeTo by Sarjen Systems on and this page was last updated .
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What is BizNET?

Sarjen Systems offers a trio of specialized, GxP-compliant solutions designed to manage the full spectrum of clinical development and laboratory operations. The first is the Early Phase CTMS (BizNET), an end-to-end software suite tailored for early-phase clinical trials and BA/BE studies. It ensures rapid, precise execution through advanced automation, barcoded trails, smart biometric identity verification, and comprehensive modules covering volunteer management, eCRF/EDC, randomization, and eTMF, alongside integrated clinical LIMS and inventory suites. Complementing this is the Late Phase CTMS (Smart Trial Suite), an advanced system built to manage complex late-phase trials by streamlining execution, enhancing patient safety, and improving adherence. This suite offers protocol-adaptive tools like IPSM for Investigational Product (IP) management, PRMS for recruitment and randomization, eTMF for central document control, eDC LP for data collection, ePRO for patient-reported outcomes, and PDMS for protocol deviation management, all while maintaining global compliance (21 CFR Part 11 & GCP). Finally, the Bioanalytical LIMS (BioLyte) provides a dedicated, specialized platform for bioanalytical laboratories. Its primary focus is to automate data review and streamline lab workflows by integrating seamlessly with instruments, ensuring end-to-end data integrity and stringent regulatory compliance (21 CFR Part 11, GLP). By reducing manual effort and errors, this LIMS solution significantly accelerates data validation, boosts productivity, and lowers operational costs for bioanalytical testing.

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