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  • Making Preclinical Data Interoperable and Regulatory Aligned: The TransSEND Approach

    Article March 23, 2026

    Preclinical toxicology studies generate an enormous amount of information: dense tables, semi-structured datasets, and long-form reports hidden away in PDFs. Turning that mix into consistent, reusable, and regulatory-ready data is often slow, expensive, and frustrating. SEND (Standard for Exchange of Nonclinical Data) was created to tackle exactly this problem. Developed by the Clinical Data Interchange […]

  • Launch of IHI JU VICT3R Initiative to Revolutionize Nonclinical Drug and Chemical Safety Evaluation with Virtual Controls

    MedBioinformatics Announces Participation in IHI JU VICT3R Initiative to Revolutionize Nonclinical Drug and Chemical Safety Evaluation with Virtual Controls

    News September 16, 2024

    [Barcelona, Spain, September 16, 2024] — MedBioinformatics today announced its involvement in the VICT3R initiative, a groundbreaking initiative aimed at transforming nonclinical drug and chemical safety evaluation. VICT3R is a public-private partnership supported by the Innovative Health Initiative Joint Undertaking (IHI JU), set to significantly reduce the number of animals used in experimental studies. The […]

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