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Health IT & Digital Health-Opinion | Op-Eds | Guest Columns | Analysis, Insights - HIT Consultant

The Market Demand for Data-Driven Tech Solutions in Healthcare

by Guilherme Macagnan, CEO, AMX Healthcare 03/06/2023 Leave a Comment

The Market Demand for Data-Driven Tech Solutions in Healthcare

The market demand for data-driven technology solutions in healthcare is on the rise. Today, one-third of the world's data is generated by the healthcare industry. This data is often complex and is coming from multiple different sources such as personal health information, claims data, clinical trial data, patient surveys, disease registries, population health statistics, wellness apps, and wearable devices. And so, the need for data management technologies continues to grow. In the Future Health
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Why Clinical Data Research Needs a Makeover in 2023

by Anne Kim, Co-Founder and CEO of Secure AI Labs (SAIL) 03/01/2023 Leave a Comment

Why Clinical Data Research Needs a Makeover

Clinical research is only as good and thorough as the data that’s available — and we need to do a better job of making that data accessible for researchers.  Unfortunately, the majority of clinical data is based on the same clinical sites and makes conclusions off a limited range of data points. Clinical trials often exclude minorities, rare disease subtypes and other underrepresented populations. Changing the way we gather and share clinical data isn’t easy. Hospitals, biobanks and
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The Rise of Fourth-Party Risk in Healthcare––And How to Combat It

by Brian Selfridge, Healthcare Cybersecurity & Risk Leader at CORL Technologies, 02/28/2023 Leave a Comment

The Rise of Fourth-Party Risk in Healthcare––And How to Combat It

In recent years, a wave of high-profile cyber attacks has shaken the healthcare industry to its core. Sensitive data has been breached; essential services have been forced offline; and healthcare providers have found themselves faced with unhappy customers and unsympathetic regulators. As a result, many in the healthcare industry are now familiar with third-party vendors and the risks they pose. This is a positive development, but it is also insufficient.
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What Impact Could AI Have On Genetic Testing?

by Dr Rocío Acuña Hidalgo, co-founder and CTO at Nostos Genomics 02/27/2023 Leave a Comment

What Impact Could AI Have On Genetic Testing?

The sequencing and analysis of human DNA have advanced significantly since the initial draft of a human genome that was published as part of the Human Genome Project. With DNA sequencing becoming increasingly cost-effective, the market for genetic testing is growing at an accelerating rate – the market for Next Generation Sequencing (NGS) services has an estimated annual growth of 18.3% from 2022 to 2030. AI presents a range of possibilities for this rapidly growing field, and in this article,
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A New Way of Thinking About Interoperability in 2023

by Stuart Hanson, CEO of Avaneer Health 02/24/2023 Leave a Comment

A New Way of Thinking About Interoperability in 2023

Interoperability in the U.S. healthcare system has been an ongoing challenge. While there are several industry initiatives that are going to advance the industry and make incremental progress toward interoperability, there remain several gaps that are unaddressed.   Interoperability is a much broader concept that encompasses more than protocols, APIs, and limited networks. It’s about more than exchanging data through one-to-one connections between a provider, payer, or vendor. True
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Addressing the Diversity Challenge in Clinical Research Through Patient Advocacy

by Andrew Barnhill, Head of Public Policy, Global Legal, IQVIA & Alexandra Weiss, Director of Strategic Partnerships, Patient Advocacy Organizations, IQVIA 02/23/2023 Leave a Comment

Addressing the Diversity Challenge in Clinical Research Through Patient Advocacy

Diversity is paramount to the success of clinical research, both ethically and scientifically. Without adequate representation of racial and ethnic minorities, investigators lack an understanding of the safety and efficacy of novel treatments within those groups. From a scientific standpoint, an incomplete dataset hinders drug delivery and the development of breakthrough therapies – but from an ethical standpoint, underrepresentation creates a barrier to treatment options for populations that
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It’s Time to Stop Accepting the Payer-Provider Dynamic as ‘Adversarial’ and Work Toward Alignment

by Heather Bassett, M.D., Chief Medical Officer, XSOLIS 02/22/2023 Leave a Comment

It’s Time to Stop Accepting the Payer-Provider Dynamic as ‘Adversarial’ and Work Toward Alignment

Today’s relationship between payers and providers is more fraught than ever. With a history of transactional, often adversarial, fee-for-service contract negotiations, it’s no wonder that the healthcare industry has grown too comfortable pitting payers and providers against each other. The lack of trust and transparency between the two groups has led to a perceived misalignment of vision. Across the board, the administrative staff has shouldered the brunt of this friction, which in the end
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How and Why Device-as-a-Service Should Be an Employee Benefit

by Falk Sonnenschmidt, SVP of Strategy at Everphone 02/21/2023 Leave a Comment

How and Why Device-as-a-Service Should Be an Employee Benefit

The Great Resignation changed how companies approach attracting and retaining talent. These days, it’s not enough to offer a competitive salary and traditional benefits like health insurance and a 401k. Employees have put an increased focus on flexibility – and the tools that support it. Phones and tablets aren’t the flashiest perk a company can offer. Still, they’re the type of lifestyle benefit that offers clear value for employees – and helps address pain points for companies
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5 Components of a Patient-Centric eCOA Strategy for Oncology Clinical Trials

by Melissa Mooney, Director of eCOA Solutions Engineering at IQVIA 02/20/2023 Leave a Comment

Amplifying the Patient Voice in Oncology Clinical Trials

In the US alone, an estimated 1.9 million new cases of cancer were diagnosed in 2022, positioning oncology as a key subject of clinical research. Throughout oncology trial development, it is important that stakeholders acknowledge that only patients can fully understand the impact of treatment on their lives. Regulators are now looking beyond clinical indications such as tumor size and delayed disease progression. When evaluating the risks and benefits of treatment, they want to know whether the
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Leveraging Technology to Bridge Gaps in Compliance

by Sean Eaton, Senior Compliance Solutions Specialist at GHX 02/17/2023 Leave a Comment

Leveraging Technology to Bridge Gaps in Compliance

American health systems, hospitals and post-acute care providers are required to comply with hundreds of regulatory requirements. Facilitating this compliance comes with a high cost. According to the American Hospital Association, the average-sized community hospital spends nearly $7.6 million annually on administrative activities to support regulatory compliance. With the impending end of the COVID-19 public health emergency set to shake up healthcare regulations, ongoing healthcare labor
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