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Conducting burden of illness studies and cost-effectiveness research is challenging without data that captures a patient’s complete journey from primary care to specialty clinics and inpatient care.

You may know you need “HIPAA compliance” to share data, but do you know how to get it, as quickly as your business needs it?

This webinar examines how enriching oncology clinical trials with real-world data generates deeper insights and improves operational efficiency to achieve better patient outcomes.

In this webinar, viewers will learn about what Datavant does and how you can enrich your dataset to get a more complete picture of your patients.

Diversity in clinical trials and clinical research needs to be improved, however, life sciences companies continue to face obstacles.

Synthetic data is the latest breakthrough in privacy-protected health data. Join a panel with Carter Prince, Head of Growth at Syntegra, Jamie Gray, Chief Operating Officer at Mirador Analytics, Su Huang, Head of Data Strategy at Datavant, and Ofer Mendelevitch, Chief Technology Officer at Syntegra in a conversation about situations where maintaining patient privacy calls for an entirely new approach – Synthetic Data. Learn more about what it is, how it’s created and when it makes sense to employ synthetic data in your health data strategy.

Connecting real world data to clinical trials holds promise for researchers and patients. It can extend the observation period of studies and supplement data for patients lost to follow up.

Decentralized clinical trials and real-world data (RWD) are two of the most commonly cited approaches for driving greater efficiency and patient-centricity in clinical research, but can they be brought together to drive even greater impact?

Effective diabetes management requires much more than tracking glucose levels. Diet, sleep, activity levels, and cardiac health all influence metabolic outcomes and outcomes in other chronic conditions.