Official-source directory
Conference Papers
13,885
available papers
10
available conferences
Papers
Showing 901–920 of 3,683
PHUSE2024·Connect·Data Science
Leveraging Open Data and Machine Learning Enhanced Data Extraction for Clinical Trials Insight ML11 EU · Strasbourg
PHUSE2024·Connect·Data Science
Topic and Sentiment Analysis of Anti-Vaccine Activism Using Natural Language Processing and Large Language Models ML12 EU · Strasbourg
PHUSE2024·Connect·Data Science
AI Got the Power: Streamlining Clinical Test Data Creation ML14 EU · Strasbourg
PHUSE2024·Connect·Data Science
Leveraging ‘Ensemble’ Machine Learning Models to Drive Automation of Specification Generation and Data Mapping in Clinical Trial Data Submission ML15 EU · Strasbourg
PHUSE2024·Connect·Data Science
Hi. I Am a Chatbot. How Can I Help You? Enhancing the Reliability and Traceability of Large Language Models ML18 EU · Strasbourg
PHUSE2024·Connect·Data Science
The Magical Trinity of TFL Automation: Digital Documents, Metadata and GenAI ML19 EU · Strasbourg
PHUSE2024·Connect·Drug Development
Harmonisation and Interoperability Between OMOP CDM and CDISC SDTM RE01 EU · Strasbourg
PHUSE2024·Connect·Drug Development
The Role of FHIR Resources in Testing and Validating an EHR to a Sponsor Data Pipeline RE01 US · Bethesda
PHUSE2024·Connect·Drug Development
Synthesised Real-world Data: JSON and the Argonauts RE02 EU · Strasbourg
PHUSE2024·Connect·Drug Development
Usage of OMOP-CDM along with CDISC in Clinical Trials: Challenges and Opportunities RE02 US · Bethesda
PHUSE2024·Connect·Drug Development
Considerations for the Submission of RWD Using CDISC, with Insights from HL7 FHIR and OMOP RE03 EU · Strasbourg
PHUSE2024·Connect·Drug Development
Future Clinical Data Submission Standards: CDISC, FHIR, OMOP, or Hybrid Model RE03 US · Bethesda
PHUSE2024·Connect·Drug Development
Ensuring Governance and Traceability of RWD from Source to Regulatory Submission: Use Case RE04 EU · Strasbourg
PHUSE2024·Connect·Drug Development
Comparing the Performance of Propensity Score Matching Algorithms from Multiple Programming Languages RE04 US · Bethesda
PHUSE2024·Connect·Drug Development
Mapping Real-World Data (RWD) to SDTM Samples for External Control Arm or Registry Studies RE05 US · Bethesda
PHUSE2024·Connect·Drug Development
Automating Real-World Data Analysis Using R Packages and Shiny: A Three-Stage Workflow RE06 EU · Strasbourg
PHUSE2024·Connect·Drug Development
Scaling ECAs from Projects to the Enterprise: Multicentre, Multisource Infrastructure for External Control Arms RE06 US · Bethesda
PHUSE2024·Connect·Drug Development
Incorporating Real-World Data in a Low-Interventional Study: Challenges and Considerations RE07 US · Bethesda
PHUSE2024·Connect·Drug Development
Future-Proofing Clinical Data Sciences: The Pivotal Role of Therapeutic Area Proficiency TA02 US · Bethesda