XBIOM™
The Clinical Data Automation Platform
Xbiom is now RAG-enabled with AI LLM technology, transforming how users access clinical trial and nonclinical study data.
Xbiom protects proprietary trial information that represents significant corporate investment and must never be exposed to external systems or cloud-hosted AI services. By deploying secure LLMs within corporate firewalls alongside the protected study data, Xbiom enables Retrieval Augmented Generation (RAG) capabilities that make stored data, information, and insights accessible through plain English queries via a Large Language Model chat interface. This approach provides instant access to data held in the deepest locations within Xbiom, making navigation intuitive for both experienced researchers and uninitiated users without specialized training.
XBIOM™ VDR, STUDY DATA I/O, CURATION
Ingest, Exchange, and Curate any Study Data Sources including EDCs and Biomarkers from Labs and/or CROs for UDM Repository
XBIOM™ MDR,
SMART TRANSFORMATION
Meta Data Repository and Automated Smart Transformation for all source and destination standards and Terminology Harmonization
XBIOM™ UDM, REPOSITORY
Universal Data Model and Future-Proofed Repository, indexed for query masks and instant search
XBIOM™ REGULATORY
Automated Generation of Submission-ready SDTM, ADaM and TFLs, eDataValidator™, SCE with R, Python programming & interface to SAS
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XBIOM™ NONCLINICAL INSIGHTS
Analytics and Visualization of all nonclinical studies sourced from LIMS , SEND, Biomarker Lab Assays, or Bio-Analytics
XBIOM™ CLINICAL INSIGHTS
Analytics and Visualization on Searchable Stratified Cohorts, On-Demand or SAP driven Statistical Analysis, Templated and Custom Plots and Tabulation, Annotated TFL objects
XBIOM™ IGO
IGO is an integrated visualization application for generating tables, listings and figures for research and publication
eDataValidator
eDV offers limitless validation of Clinical SDTM and ADaM as well as Nonclinical SEND, making this a single solution for IND, NDA and BLA preparation
Comprehensive Clinical Data Automation Platform (CDAP)
for Global BioPharma
At PointCross, we deliver cutting-edge technology solutions designed to streamline all aspects of Clinical Data Automation for the global BioPharma industry. Our robust CDAP platform offers:
Data Management and Curation
Efficiently handle and organize clinical data
Future-Proofed Warehousing
Secure and scalable storage solution
Standardization and Harmonization
Ensure compliance with regulatory submission standards.
Advanced Analytics and Visualization
Transform data into actionable insights
News & Announcements
SOT 65th Annual Meeting and ToxExpo
Date: March 22–26, 2026
Location: San Diego, California
PointCross will be attending the Society of Toxicology (SOT) 65th Annual Meeting and ToxExpo in San Diego. Visit us at Booth #2107 to learn how Xbiom™ Single-Track is helping nonclinical CROs accelerate study report delivery and automatically generate SEND datasets.
We will also host an Exhibitor Session titled “Automating Study Report and SEND Integration in Nonclinical Safety Studies” on Monday, March 23, 2026, from 3:15–4:15 PM.
Learn More
PointCross to Present at PHUSE US Connect 2026
Date & Time: Monday, March 23 | 1:30 PM – 2:00 PM
PointCross will attend PHUSE US Connect 2026 in Austin, Texas (March 22–26, 2026).
Rahul Madhavan will present “V03: Optimizing the Use of Data Standards” during the Advance Session: Building a Better MDR, alongside collaborators from Merck and Daiichi Sankyo
PointCross at Phuse APAC Connect 2026
Event Date: 19–21 February 2026
Location: Hyderabad, India
PointCross Life Sciences participated in PHUSE APAC Connect 2026, held from 19–21 February 2026 in Hyderabad, India. The event brought together global leaders across clinical data science, innovation, and regulatory standards, alongside India CDISC Day, uniting two influential data standards communities under one platform.
Press Release
Dec 18, 2025, 11:30 ET
PointCross Revolutionary Single-Track Process Transforms Nonclinical Data Management
PointCross Sponsors PHUSE SDE Bengaluru 2025
Event Date: Saturday, 22 November 2025
Location: Bengaluru, India
Our experts, Haris Khan and Arpitha Hanumanthaiah, delivered the session “From Protocol to SDTM: Automating Trial Design with Large Language Models,” showcasing how PointCross is advancing automation in clinical data workflows.
Learn More: PointCross at PHUSE SDE Bengaluru 2025 – Gold Sponsor
PHUSE EU Connect 2025
Event Date: 16 – 19 November 2025
Location: Hamburg, Germany
At PHUSE EU Connect 2025, Harinarayan Gopichandran, VP Technical Solutions from PointCross demonstrated how the 𝐗𝐛𝐢𝐨𝐦 𝐒𝐦𝐚𝐫𝐭 𝐌𝐞𝐭𝐚𝐝𝐚𝐭𝐚 𝐑𝐞𝐩𝐨𝐬𝐢𝐭𝐨𝐫𝐲 (𝐌𝐃𝐑) helps Sponsors and CROs streamline clinical trial setup, automate metadata governance, and improve consistency across studies.
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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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