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December 21, 2017
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From 102 patients in the first year of operation to more than 1.6 million patient-visits last year, St. Joseph's continues to evolve as the leading health resource in the community and for the community.
whitePaper | February 14, 2023
Capturing and combing through various data sets can be overwhelming, especially in today’s clinical trial environment. An end-to-end data environment creates new opportunities.
whitePaper | November 17, 2021
The pandemic hit the healthcare industry hard, but it also weakened the cybersecurity defenses of most providers, making them far more vulnerable to threats such as ransomware. This report, covered across national news, is considered the most significant actionable cybersecurity research over the past several years because it also documents the severe impact on patient care. This executive summary includes critical areas that providers can address starting today.
whitePaper | October 21, 2021
This whitepaper reveals the role of customer operations in helping healthcare organizations deliver top-notch patient experiences, control costs, and boost efficiency — highlighting the key pillars top performers use to attain their service and back-office objectives.
whitePaper | February 4, 2020
When it comes to electronic medical records (EMR) software, it’s important to find the system best fit for your businesses’ needs, goals, and budget. This guide written by Software Advice, covers everything you need to know about software pricing in 2020. Compare pricing models, price ranges, popular system prices, and unexpected costs of EMR software. In addition to your download, you’ll be able to chat with an advisor in your industry and get personalized software recommendations.
whitePaper | September 28, 2022
Specialty drugs span a wide range of disease states, from the more prevalent, yet complex, such as multiple sclerosis, to rare and orphan diseases, such as hereditary angioedema (HAE).
whitePaper | March 23, 2023
DCTs can take a variety of forms depending on patients’ needs, study protocol, drug company preferences, or regulatory requirements. Trials may be remote and decentralised from start to finish with no physical contact between participants and investigators or they may rely on hybrid designs that incorporate only certain elements of decentralisatio
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