As healthcare employment trends change, hospitals are being forced to change their physician recruitment strategies, too. New myriad influences demand that facilities do more to attract the best ...

Please provide your email address to receive an email when new articles are posted on . Clinical registries “will be able to influence care profoundly” in the future and will complement, rather than ...

Data captured in NCDR registries is similar in quality, depth and granularity when compared to data captured through clinical trials, according to research in JACC: Cardiovascular Interventions that ...

The Department of Health and Human Services could improve Medicare quality through its clinical data registry program if it concentrated on performance measures, concluded a new federal report ...

A clinical data registry tracks information about the health status of patients and the care they receive over a period of time. Registries can be focused on a specific diagnosis or condition and ...

For companies developing marketing authorization applications (MAAs) for recombinant and human plasma-derived factor VIII and factor IX hemophilia medicines in previously untreated patients (PUPs), ...

Natural Language Processing Algorithm to Extract Multiple Myeloma Stage From Oncology Notes in the Veterans Affairs Healthcare System Real-world data (RWD) collected on patients treated as part of ...

The ongoing transformational shift to value-based payment in healthcare is fueling the rise of clinical data registry participation. The average U.S. healthcare facility participates in five to 10 ...

The GI Quality Improvement Consortium, a partnership between the American College of Gastroenterology and the American Society of Gastrointestinal Endoscopy, is moving to a new technology platform ...

With the introduction of seven new disease-specific registry datasets, Veradigm is enabling deep, targeted research to drive innovation and enhance real-world clinical insights Veradigm’s Clinical ...

A review of clinical registries determined data collection on patient outcomes are substandard and the information is not useful for patients, physicians, and policy makers, according to a paper ...