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Clinical SolutionsClinical Trial & Molecular Biomarker Research

Semantically harmonize and integrate all your data from clinical trials, molecular and immuno biomarkers, bio-sample availability and bioinformatics into Xbioms’™ searchable warehouse with a universal data model to find cohorts, signals or do analytics across domains.

Clinical SolutionsClinical Metadata Governance & Regulatory Compliance

Manage CDISC standards driven metadata and data models for all stages of clinical trials from protocols to eCRF to submission with validated workflows. Xbiom lets sponsors specify data models and receive studies from CROs in SDTM, to validate and package technically conformant clinical data for regulatory submissions to the FDA and PMDA.

Nonclinical SolutionsNonclinical Cross-Study Analytics & Warehousing

Semantically harmonize and combine all your Nonclinical study data into Xbioms’™ searchable warehouse with a universal data model to find subjects, dose groups or studies that show safety signals or patterns of interest for analysis and cross domain views.

Nonclinical SolutionsXbiom Nonclinical Regulatory Submissions & Study Lifecycle

Workbench for all practicing regulatory and data management teams at sponsors. Xbiom Nonclinical Regulatory Submissions and Study Lifecycle Solutions is offered as a Software as a Service on the AWS cloud, and is validated and qualified for regulatory use.


Success For Our Valued Customers

We thank our customers for their trust shown in us and take pride in our accomplishments.

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