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PointCross SitemapGeetha2026-06-02T07:25:06+00:00
Posts
- The Business Case for Automating Nonclinical Study Reports (June 3, 2026)
- FDA SEND Requirements for Nonclinical Studies: Which Studies Need SEND Datasets in 2026? (May 20, 2026)
- AI in Nonclinical Reporting: From Hype to Real Workflow (May 19, 2026)
- SEND Dataset Quality: Why Passing the Validator Is Only Half the Battle (May 11, 2026)
- What the FDA's TCG v6.2 Update Means for Your SEND Deliverables (April 28, 2026)
- Welcoming PingPing Gong to PointCross (April 21, 2026)
- Webinar- Automating Study Report and SEND Integration in Nonclinical Safety Studies (April 1, 2026)
- Three Steps to Transforming CRO Productivity: Time, Cost, and Quality in Nonclinical Study Reporting (March 17, 2026)
- PointCross at PHUSE US Connect 2026 (March 13, 2026)
- SOT 65th Annual Meeting and ToxExpo (March 12, 2026)
- PointCross at Phuse APAC Connect 2026 (February 12, 2026)
- Revolutionary Single - Track Process Transforms Nonclinical Data Management (December 19, 2025)
- Does my Study need SEND? (November 24, 2025)
- PHUSE EU Connect 2025 (November 14, 2025)
- Refreshing Clinical Data Validation for Modern BioPharma (November 14, 2025)
- PointCross at PHUSE SDE Bengaluru 2025 - Gold Sponsor (October 31, 2025)
- Metadata Repository: Your Strategic Edge in Clinical Development (October 21, 2025)
- Bridging the Gap: How Natural Language AI Can Transform Clinical Data Access (October 8, 2025)
- Ask with Ease. Retrieve with Rigor. Study Data Secured by RAG-Enabled Chat in Xbiom (September 17, 2025)
- How Leaders Can Shape Drug Success Through Data (September 4, 2025)
- The Hidden Bottleneck Undermining Pharma's Mission (August 28, 2025)
- The AI Revolution CMOs & CSOs Need Now (August 20, 2025)
- Enterprise LLMs for BioPharma Therapeutics Development (August 13, 2025)
- PointCross at PHUSE SDE 2025 – South San Francisco (August 8, 2025)
- Breaking Free from Clinical Data Chaos: The AI Revolution CMOs & CSOs Need Now (August 8, 2025)
- Bridge Over Troubled Data: How RAG Connects AI Dreams to BioPharma Reality (July 23, 2025)
- Achieving 100% Data Quality in SEND Submissions with SEND Assure (July 3, 2025)
- PointCross Life Sciences is a Ruby Sponsor of CDISC India Day 2025 (July 3, 2025)
- Redesigning the Pipeline: Smarter Data for Strategic Advantage (July 3, 2025)
- Shivakumar Swamy Joins PointCross as Head of Quality & Compliance (June 18, 2025)
- PointCross Sponsors PHUSE SDE Hyderabad 2025 (June 12, 2025)
- Webinar: Ensuring 100% Submission Data Quality with SEND ASSURE (May 14, 2025)
- Webinar- Automating Biomarker Standardization: Highlighting best practices for the Cell Phenotyping (CP) domain (April 3, 2025)
- PointCross at PHUSE APAC SDE 2025 (March 25, 2025)
- PHUSE US Connect 2025 (February 20, 2025)
- SOT 64th Annual Meeting (February 20, 2025)
- Bay Area Biotech-Pharma Statistics Workshop (BBSW) (October 14, 2024)
- Streamline Clinical Data Management Across Collection, Exchange, Analysis & Reporting with Xbiom™ MDR (September 25, 2024)
- Hexaware Launches Clinical Data Automation as a Solution (CDaaS) in Partnership with PointCross Life Sciences (September 24, 2024)
- Unlocking Insights: Cross-Study Analysis of SEND Datasets with Xbiom™ (September 13, 2024)
- Webinar on Visualization of SEND datasets (August 19, 2024)
- Clinical Research Metadata Management Repository : The Role of Xbiom by PointCross (June 26, 2024)
- Webinar on The Most Common Issues in Preparing SEND: Explained (May 31, 2024)
- PointCross attends Verisian first community event in Hyderabad (May 6, 2024)
- SOT ToxExpo 2024 (March 18, 2024)
- Interim Nonclinical Study Monitoring with Xbiom™ Insights (February 15, 2024)
- PHUSE US CONNECT 2024: PointCross Highlights Rapid SDTM and Compliance Dashboards (January 18, 2024)
- SCOPE Summit for Clinical Ops Executives 2024 (January 18, 2024)
- Clinical Interim Study Monitoring: A Deep Dive into PointCross Xbiom™ Insights (January 9, 2024)
- From FAIR Data to FAIR Knowledge Sharing (December 16, 2023)
- 10 Most Recommended Pharma & Life Sciences Technology Companies - 2023 (November 21, 2023)
- Enhancing Clinical Trial Data Integrity Through Automation (October 3, 2023)
- Exchange Clinical data with SDTM, but analyze it on a Unified Repository (August 25, 2023)
- Validation for Clinical SDTM, ADaM, and Nonclinical SEND Data (August 21, 2023)
- PHUSE SDE 2023 (July 18, 2023)
- SEND Data Standardization: Streamlining Nonclinical Study Submissions for FDA Approval (July 3, 2023)
- Clinical Trials: Understanding the Basics, Types, and FAQs (June 13, 2023)
- eDataValidator for SDTM, ADaM & SEND (May 25, 2023)
- PointCross Incorporates PMDA Validation Rules V4 (May 2, 2023)
- SDTM Automation: Streamlining Clinical Trial Data (March 13, 2023)
- EDC Raw Data to SDTM Curation, Mapping and Automation with the Xbiom Tool (March 7, 2023)
- Webinar on Harmonizing Raw Data with CDISC Standards to Streamline SDTMs (January 11, 2023)
- Clinical and Nonclinical validation Tools (January 10, 2023)
- FDA SEND Dataset Services (January 2, 2023)
- SDTM - Everything that you need to know (December 26, 2022)
- Universal Data Model - PhUSE Americas Winter SDE (December 8, 2022)
- PointCross announces full complement release of eDataValidator (July 25, 2022)
- PointCross releases eDataValidator for SDTM, ADaM, SEND, and Define.XML conformance to prevailing FDA, CDISC, and PMDA rules (July 14, 2022)
- Incorporating Histopathology data of organs and tissues for terminal subjects from a draft PDF report (February 2, 2022)
- Sponsor conducting Xenograft studies on a tumor growth (February 2, 2022)
- Delayed PK data hampers clinical assessment (February 2, 2022)
- Case Study: Business Benefits from Monitoring of Ongoing Studies (February 2, 2022)
- Interim Study Monitoring Webinar (September 22, 2021)
- Orchestra™ (May 25, 2021)
- SRR Files & Template (May 25, 2021)
- Case Study: Integrated Repository of Nonclinical Studies (May 25, 2021)
- Enabling Data Integration for Translational & Precision Medicine (May 7, 2021)
- Beginning on September 15, 2021, FDA will begin enforcing the Technical Rejection Criteria (TRC). (March 25, 2021)
- SEND DART is now supported by PointCross Life Sciences (March 25, 2021)
- FDA to enforce the Technical Rejection Criteria (TRC) beginning Sept 15th, 2021 (March 25, 2021)
- Tri-Con of Molecular Medicine (February 17, 2021)
- Conference: PhUSE SDE - Canton, MI (January 15, 2021)
- PhUSE CSS 2020 Poster (January 15, 2021)
- Taking full advantage of the SEND data potential (January 15, 2021)
- Visualization of “Real Time” Data from Ongoing Non-Clinical Studies in Support of Study Monitoring and informed Decision Making (January 15, 2021)
- Validation Consistency and Conformance of SEND Datasets (January 14, 2021)
- PhUSE EU Connect: Amsterdam (January 14, 2021)
- Xbiom Workbench and Insights (January 14, 2021)
- Xbiom Smart Transformer - Demo (January 14, 2021)
- Xbiom Accelerating Innovation in BioPharma (January 14, 2021)
- Unified Machine Readable Target Data Models from Smart Transformer of Disparate Biopharma Source Data (January 14, 2021)
- SEND Dataset FRR Webinar: Tools & QC Checks (January 14, 2021)
- 100% Consistency Check of SEND Datasets Against NCSR (January 14, 2021)
- PhUSE Single day event (September 11, 2019)
- Streamlining Sponsor’s Nonclinical & SEND Outsourcing to CROs (May 20, 2019)
- Xbiom– A Workbench for Biomarker & Translational Research (May 20, 2019)
- A Workbench for Biomarker and Translational Research (May 17, 2019)
- PhUSE 2019 Computational Science Symposium (May 17, 2019)
- Bayer Data Insights Event Berlin (April 20, 2019)
- Xbiom: Translational & Biomarker Research Workbench (April 20, 2019)
- Bio-IT World Conference an Expo – 2019 (April 11, 2019)
- Workshop: A Workbench for Biomarker and Translational Research (April 11, 2019)
- Smart Transformer of Clinical & Nonclinical Data for Insights (April 11, 2019)
- Face-to-Face CDISC SEND at FDA (April 11, 2019)
- Phuse SDE (April 4, 2019)
- Xbiom: Biomarker Workbench for BioTech & Pharma (February 16, 2019)
- PointCross Live Discussion - Recent Regulatory and Standards Updates (December 13, 2018)
- PhUSE Connect EU – The Clinical Data Science Conference (August 29, 2018)
- PhUSE paper- Ensuring consistency of SEND Datasets with Study Reports using Machine Learning Algorithms (February 23, 2018)
- Ensuring consistency of SEND Datasets (February 23, 2018)
- The Molecular Medicine Tri Con Conference 2018 (February 8, 2018)
- PhuSE Single Day Event Foster City (February 8, 2018)
- PhUSE CSS Computational Science Symposium (January 30, 2018)
- Benchmark your SEND Readiness (January 29, 2018)
- Benchmark Your SEND Readiness Whitepapers (January 23, 2018)
- Standards and Ontology Driven Workflow Automation of Clinical Studies (October 11, 2017)
- Synthetic Dataset (September 13, 2017)
- Integrating Clinical, Biomarker & Disparate Data (May 22, 2017)
- PointCross Inks two deals for its Xbiom™ Insights – Clinical Biomarker Platform for Precision Medicine Development (February 15, 2017)
- Introducing PointCross Desktop Validator (January 19, 2017)
- SEND ASSURE™ Whitepaper (November 8, 2016)
- Data Standardization Services (November 8, 2016)
- Xbiom™: Precision Medicine Biomarker Research (September 9, 2016)
- Integrated Repository of Nonclinical Studies: A Case Study for a Centralized, Searchable Registry of all Nonclinical Studies for Drug Safety and Toxicology Research (June 13, 2016)
- Data Consistency and Quality Issues in SEND Datasets (June 2, 2016)
- CIMS™: Clinical Data Repository for SDTM Data & Beyond (March 14, 2016)
- PointCross Life Sciences and Xybion forge strategic partnership to deliver SEND services to assure FDA review ready submissions (March 11, 2016)
- Importance of Data Consistency and Quality in SEND Submissions (March 5, 2016)
- Semantic Data Exchange for Pharma R&D (November 21, 2015)
- PointCross & CAC EXICARE Partner for CDISC Implementation (August 24, 2015)
- PointCross and InterpretOmics partner for Clinical and Genomic Biomarker Management for Drug Development (April 20, 2015)
- PointCross Life Sciences Announces SaaS Environment for FDA Nonclinical Study Data Reviewer Analytics and Submissions (June 6, 2013)
- PointCross Life Sciences: Gartner Cool Vendor 2013 (May 17, 2013)
- PointCross Life Sciences - Get SEND Ready Today (May 2, 2013)
- What does SEND Readiness mean for your company? - Webinar (June 27, 2012)
- Study Data Integration & Search (SDIS™) Demo (October 6, 2011)
- Streamline Study Data Integration with SD (September 26, 2011)
Pages
- PointCross Sitemap (June 2, 2026)
- Chinese Pages (May 20, 2026)
- eDataValidator (May 11, 2026)
- SEND 数据集生成 (May 11, 2026)
- 数据标准化服务 (May 11, 2026)
- Single Track File (February 3, 2026)
- Single Track Processing (January 27, 2026)
- ContentOracle AI Chat Results (January 13, 2026)
- test (January 13, 2026)
- IGO – IMMERSIVE GRAPHICS OBJECT (August 14, 2025)
- Quality Policy (May 30, 2025)
- Information Security Policy (May 30, 2025)
- ADaM for Clinical (December 18, 2024)
- SEND ASSURE and Corrections (November 28, 2024)
- Clinical Data Management (October 8, 2024)
- XBIOM™ Regulatory Submission (August 19, 2024)
- XBIOM™ UDM, Repository (August 19, 2024)
- XBIOM™ Virtual Data Room for Data Exchange & Curation Tools (August 19, 2024)
- Partners (June 13, 2024)
- Digitization, Analysis and Warehousing of Legacy Clinical Trial Data (August 11, 2023)
- Phuse SDE (July 27, 2023)
- Code of Conduct and Code of Ethics (May 4, 2023)
- XBIOM™ Metadata Repository, Smart Transformer, and eDataValidator (February 19, 2023)
- Harmonizing Raw Data with CDISC Standards to Streamline SDTMs (January 19, 2023)
- SEND Generation and SEND QC Indicative Quote Generation (November 22, 2022)
- eDataValidator (November 15, 2022)
- Automated SDTM Generation from EDC (September 20, 2022)
- DATA CONCIERGE – Clinical & Translational (July 1, 2022)
- DATA CONCIERGE – Nonclinical (July 1, 2022)
- Data Quality Assurance (July 1, 2022)
- Biomarker Assays (July 1, 2022)
- Data Standardization Services (July 1, 2022)
- Clinical or Nonclinical Repository, Search, Analytics and Visualization (June 30, 2022)
- Biosample Tracking for Specialty Assays – Translational Medicine (June 30, 2022)
- Interim Nonclinical Study Monitoring (June 30, 2022)
- Data Services (June 9, 2022)
- Digital Study Report (June 9, 2022)
- SEND ASSURE: 100% QC of PREPARED SEND DATASETS (June 9, 2022)
- SEND GENERATION (June 4, 2022)
- Software License Agreement - PointCross Life Sciences (March 4, 2022)
- Interim Study Monitoring Pricing (February 3, 2022)
- Conferences and Events (September 22, 2021)
- Monitoring Clinical Trials with Interim Data (September 21, 2021)
- Thank You PointCross (August 18, 2021)
- Direction to PointCross Office in Bangalore, India (June 16, 2021)
- Directions to PointCross Foster City office (June 16, 2021)
- PointCross (June 3, 2021)
- Request a Demo (May 27, 2021)
- Clinical Resources (May 24, 2021)
- Nonclinical Resources (May 24, 2021)
- All Resources (May 24, 2021)
- Orchestra™ & SOLO™ (May 24, 2021)
- Case Studies (May 24, 2021)
- SRR Files & Template (May 24, 2021)
- Our commitment to Data Security & Privacy (May 24, 2021)
- PointCross Privacy Policy (May 20, 2021)
- PointCross Blog (May 19, 2021)
- Data Concierge Service (May 19, 2021)
- Smart Transformer (May 19, 2021)
- INTEGRATED GRAPHICS OBJECT (IGO) & INSIGHTS – Nonclinical (May 19, 2021)
- XBIOM™ REGULATORY WORKFLOWS AND TOOLS (May 19, 2021)
- INTEGRATED GRAPHICS OBJECT (IGO) & INSIGHTS – Clinical Trials & Biomarkers (May 19, 2021)
- XBIOM™ (May 19, 2021)
- Careers at PointCross (May 15, 2021)
- About PointCross (May 15, 2021)
- Blogs (June 20, 2016)
- Contact Us (June 14, 2016)
Conferences and Events
- Panel Discussion: Empowering Toxicologists with Access to Near-Real Time Study Data through Interim Study Monitoring: The Sponsor’s Perspective (March 10, 2022)
- PhUSE US Connect-2021 (July 8, 2021)
- Bayer Data Insights Event (May 31, 2021)
- PhUSE US Connect (May 31, 2021)
- CDISC SEND Face to Face at FDA (May 31, 2021)
- Phuse SDE 2019 (May 31, 2021)
- Bio-IT World Conference an Expo – 2019 (May 31, 2021)
- AWS and PointCross Workshop at Boston (May 31, 2021)
- PointCross and AWS Workshop (May 31, 2021)
- Smart Transformer of Disparate Data Into Unified Form (May 31, 2021)
- PhUSE CSS in Silver Spring, MD (May 31, 2021)
- 15th annual biomarker world congress (May 31, 2021)
- Converting Biopharma Source Data to Unified Models (May 31, 2021)
- PhUSE Single day event: Beerse, Belgium (May 31, 2021)
- PhUSE EU Connect: Amsterdam (May 31, 2021)
- Webinar – The release of the PointCross eDataValidator (May 31, 2021)
- Webinar: Additional Tools and QC checks to ensure SEND datasets are Fit For Review (FRR). (May 31, 2021)
- PHUSE US Connect 2020 (May 31, 2021)
- PhUSE CSS 2020 Poster (May 31, 2021)
- PHUSE CSS 2020 (May 31, 2021)
- FDA to enforce the Technical Rejection Criteria (TRC) beginning Sept 15th, 2021 (May 31, 2021)
- Webinar Recording: Enabling Data Integration for Translational & Precision Medicine (May 31, 2021)
- Effective March 15, 2021: Support for SEND DART IG 1.1 per FDA Data Standards Catalog (May 31, 2021)
- Molecular Medicine Tri-Con (February 17, 2021)
- Conference: PhUSE SDE – Canton, MI (September 29, 2020)