2024 - How EHR Data Can be Used to Advance Guideline-directed Care
Date2024-12-05
Deadline2024-12-05
VenueONLINE-VIRTUAL, USA - United States
KeywordsLife Sciences; Clinical Trials; Pharmaceutical
Topics/Call fo Papers
Understanding post-approval performance of medical devices is inherently challenging whether through randomized trials or real-world data (RWD). Device researchers are often limited to studying broad device classes or setting up agreements with individual providers or health systems to collect necessary data.
In this webinar, the expert speakers will have an in-depth discussion on advancing medical device performance and patient outcomes using complete electronic health records (EHR) data. They will share insights into their partnership to address gaps in real-world device performance data, foster innovation, promote health equity and inform clinical guidelines.
The understanding of post-approval medical device performance can be revolutionized by providing access to complete EHR data, including device-level data, clinical notes and medical images, for more than 100 million patients. These data can be standardized to a common model, linked across health systems and enriched with social determinants of health, mortality and claims data for a holistic view of patient journeys.
In this webinar, the speakers highlight published research using data on device utilization and safety for peripheral artery disease and pulmonary embolism as well as discuss how future research and research collaborations can be conducted using standardized data models.
Register for this webinar today to discover how complete EHR data are advancing medical device performance and improving patient outcomes.
Keywords: Clinical Research, CRO, Digital Health, Medical Devices, Market Access, Clinical Data, Clinical Development, HEOR, RWE, Commercialization/HEOR/Market Access, RWD
In this webinar, the expert speakers will have an in-depth discussion on advancing medical device performance and patient outcomes using complete electronic health records (EHR) data. They will share insights into their partnership to address gaps in real-world device performance data, foster innovation, promote health equity and inform clinical guidelines.
The understanding of post-approval medical device performance can be revolutionized by providing access to complete EHR data, including device-level data, clinical notes and medical images, for more than 100 million patients. These data can be standardized to a common model, linked across health systems and enriched with social determinants of health, mortality and claims data for a holistic view of patient journeys.
In this webinar, the speakers highlight published research using data on device utilization and safety for peripheral artery disease and pulmonary embolism as well as discuss how future research and research collaborations can be conducted using standardized data models.
Register for this webinar today to discover how complete EHR data are advancing medical device performance and improving patient outcomes.
Keywords: Clinical Research, CRO, Digital Health, Medical Devices, Market Access, Clinical Data, Clinical Development, HEOR, RWE, Commercialization/HEOR/Market Access, RWD
Other CFPs
- Early Access Programs – The Definitive Test for Guiding Pharma’s Commercialization Strategy
- How Oncology Biotechs Can Achieve Always Audit Ready Clinical Operations
- Targeted Therapies: The Role of Large Molecules, Biologics and ADCs
- Moneyball for Drug Development: How Causal Inference can Increase the Probability of Success in Clinical Trials
- Utilizing the Measurement of Cognition to Determine Drug Safety in Late Phase Clinical Trials
Last modified: 2024-10-16 04:55:26