The
XBIOM™ PLATFORM
XBIOM™ NONCLINICAL INSIGHTS
Longitudinal integration of disparate components of nonclinical studies into a repository for search and discovery of signals or cohorts based on specified criteria.
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XBIOM™ CLINICAL INSIGHTS
Clinical trial repository with longitudinally integrated biomarker assay data for analytics and visualization of ongoing or completed trials.
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XBIOM™ REGULATORY
Regulatory workflows and tools for the gathering, preparation, validation, and packaging of submissions to regulatory agencies.
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XBIOM™ SMART TRANSFORMATION
Rapidly map legacy and raw data to universal data model, regulatory, industry, or de-facto standards.
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News & Announcements
Webinar on "Visualization of SEND datasets"
July 31st 2024
Join us for a follow up webinar, Visualization of SEND datasets on July 31st at 09:00am PT / 12:00pm ET. As part of the industry's leading nonclinical study repository, we are committed to helping you get the most out of your SEND datasets.
Webinar
May 29, 2024
The Most Common Issues in Preparing SEND: Explained
PHUSE SDE
Gurugram, India
March 16th, 2024
The discussions revolving around “Data Standards, Metadata, Automation, and Technology” were incredibly enlightening, underscoring the significance of leveraging data strategically for unlocking business value.
SOT ToxExpo 2024
Salt Palace Convention Center
in downtown Salt Lake City, Utah
Date: March 10–14, 2024
Here are the takeaways:
- CROs and Sponsors love PointCross’ instant SEND quote generator, fast turnaround time, and study data visualization offering
- Integrating bioanalytical and complex biomarker data with as collected in-life data can be done in real time and people loved seeing subject level study details for ongoing study monitoring!
Phuse US Connect 2024
Date: February 25–28, 2024
Bethesda, Maryland, USA
PointCross Life Sciences was thrilled by the level of interest and excitement with regards to the poster we presented at PhUSE Connect 2024, titled “Rapid SDTM and Compliance Dashboards”. We had some important dialogue with industry peers and leaders in the space pertaining to revolutionizing SDTM development in clinical research. Learn more
View our poster: Effective WorkFlow Process: Rapid SDTMs and Compliance Dashboards
Read our paper: Paper PP29 Effective WorkFlow Process: Rapid SDTMs and Compliance Dashboards
Driving
Success For Our Valued Customers
We thank our customers for their trust shown in us and take pride in our accomplishments.
US – India – Europe
Our Vision
Our Vision is to standardize and contextually integrate all data collected in discovery or nonclinical and clinical trials, with genomic and immune response data from the patient from their bio-samples or other, to support precision medicine development and translational research to discover treatments for illness and disease.
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