Join nearly thirty industry organizations who have adopted HL7 Vulcan standards into their systems to enable the clinical research infrastructure. Watch as these Vulcan stakeholders weave together the technical protocols and solutions that will advance cancer use cases, clinical trial readiness projects, health equity, and together build a stronger clinical trials infrastructure.
- See nearly 30 organizations share live demonstrations of pre-pilot implementations using HL7® FHIR®
- Join the clinical research community to provide feedback, questions and comments on end to end FHIR workflows
- Learn where to find the resources you need to use FHIR APIs to improve data quality, efficiency, and overall cost to conduct research
Vulcan Interoperability Bridge Event Demonstration Focus Areas
Internal Sponsor Systems:
This focus area is dedicated to life sciences organizations who are focused on research and development information exchange. Demonstrating the use of HL7 FHIR to digitize clinical protocols and structure schedules of activities within a life sciences company or other clinical trial sponsor organization.
Research Site to Sponsor:
Watch as two different implementation teams demonstrate how to enhance data accessibility, streamline processes, and accelerate research timelines to deliver substantial ROI for clinical research sites and sponsor organizations by improving interoperability among electronic data capture systems.
Product Labeling:
As a first step toward streamlining the ability to support rapid investigation of new or increased adverse events related to medical products, structured drug labeling information is a critical advancement. With structured labels that include sections such as structured adverse reaction section and ingredients, adverse events related to medical products can more easily be updated and discovered.
Patient Driven Information Exchange:
Explore ways to engage patients to allow them to directly share their RWD (EHR data, PROs, AE, etc.) with clinical research. Patient engagement gives sponsors and CROs an opportunity to gain invaluable data input and feedback from stakeholders who have traditionally not been viewed as a core part of the study team – patients.
Health Information Exchanges:
Data is often contained in separate sources utilizing different schema and coding, requiring significant workload to harmonize the data, creating a longitudinal record across various systems. This team of HIEs will demonstrate how they allow federated data compilation into a single set that can be used for real-world research questions that are approved by an honest broker.