One repository for the entire study data lifecycle
The XBIOM™ Repository holds all study data in a future-proofed, normalized Unified Data Model, harmonized to a global terminology set and mapped to de jure controlled terminology for exchange.
All study data, normalized and harmonized
The XBIOM™ Repository holds all study data managed by XBIOM, normalized to a simple data model and harmonized to a global terminology set mapped to de jure controlled terminology used when exchanging data. The studies include in-vitro and specialty assays from bio-banked bio-samples, in-vivo animal study data, and clinical trial data.

Built for access, transformation & search
XBIOM’s UDM accommodates the longitudinal representation of as-collected data along with an unlimited number of metadata and derived metadata. These serve various planned and ad hoc access or transformation needs, such as standardization for the exchange of data to external agencies.
- ✓ Longitudinal as-collected data with unlimited metadata and derived metadata
- ✓ Indexed to serve search queries across disparate data domains
- ✓ Query masks that are hierarchical and recursively applied for evolving repositories
- ✓ On-demand standardization for exchange to external agencies
From bio-samples to clinical trials
UDM manages large volumes of specialty biomarker assays and integrates them longitudinally with in-vivo and clinical data.
Biomarker Assays
Large amounts of specialty biomarker assay data, especially valuable when longitudinally integrated to the patient’s in-vivo data from clinical trials.
In-vivo & In-vitro
In-vivo animal study data and in-vitro specialty assays from bio-banked bio-samples. Large BioPharma companies use UDM to hold all their safety study data from animal studies.
Clinical Trial Data
Patient data from clinical trials, integrated longitudinally with biomarker and in-vivo data to support cross-study research and submission-ready standardization.
Powering the full data lifecycle
The UDM repository is the keystone of the entire lifecycle of clinical and study data, from legacy studies to ongoing ones.
Ad hoc research insights
Serve ad hoc research for insights, drawing on a unified longitudinal view of subjects across studies and data domains.
Submission-ready standardization
Produce submission-ready standardization using CDISC SDTM and ADaM, exported directly from the harmonized repository.
Exploratory cross-study research
Leverage search and analysis across studies, from legacy to ongoing, for exploratory research and discovery.
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