International Conference on Clinical Data Mining - (ICCDM-25)


2nd - 3rd August, 2025 | Ottawa, Canada

Multi-format (In-person/Virtual)

Important Dates

Pre-registration Deadline

3rd July, 2025

Paper Submission Deadline

13th July, 2025

Last Date Of Registration

18th July, 2025

Date Of Conference

2nd - 3rd August, 2025

Downloads

Call For Paper

The Research Leagues events aim to release a wide range of articles that provide insight and explore the latest advancements in engineering, medicine, social science, applied science, management etc.

Our conference practices methodological, conceptual, and epistemological diversity. But we prefer articles that effectively engage with current intellectual debates. We expect our participants to contribute innovative ideas, perspectives, and research methods.

Our events can potentially revolutionize the current paradigm and pave the way for growth and development. Those who intend to have their original findings and research published through our events should get an idea from the Author Guidelines, Rules for Presentation, and Instruction sections, before anything else.

Engineering

  • Clinical data warehouse
  • Clinical data repository
  • Potential uses of a clinical data warehouse
  • Research issues in clinical data warehousing
  • Medical data mining
  • Development of a clinical data warehouse
  • Clinical data warehouse issues and challenges
  • Warehouse architecture for clinical data warehousing
  • Clinical document data warehouse
  • Data standardization
  • Data warehouse design methods
  • Patient demographics
  • Booking information
  • Case record data
  • Surgical procedure data
  • Visit location
  • Insurance information
  • Patient and provider contact data
  • Diagnosis
  • Patient contact information
  • Appointment information
  • Recurring reports
  • One time data sets
  • Online reports
  • Data counts
  • Cross-referenced data
  • Ongoing medical review
  • Data cleaning
  • Data reconciliation
  • Streamlined statistical analysis for
  • Submission
  • Protocol design and trial simulation
  • Responding to regulatory queries
  • Safety monitoring and signal detection
  • Cross-study analysis
  • Single data storage for visualization/analysis tools

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