Webinars2018-10-02T21:10:08+00:00

Prometheus Research and Compliancy Group joined forces for the second webinar in the series: The Next Healthcare Registry Frontier. We focus on the noteworthy changes to the Common Rule, how they will impact academic researchers and clinical caregivers, and, more importantly, the steps to take to take advantage of the opportunities in the future.

Length: 40 minutes plus Q&A

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Leveraging data outside of the traditional care continuum can unlock valuable insights for use in risk adjustment, population-based patient management, and patient-provider engagement. Learn about important considerations and opportunities for enhancing your QI initiatives with data from research, patient-reports, and other non-traditional channels.

Length: 45 min

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Is your registry fulfilling its promise of creating a virtuous cycle of performance improvement in your discipline? Many registries have achieved their initial goal of facilitating participation in CMS incentive payment programs, yet most formal and informal discussions at NQRN 2017 were dominated by the challenges stewards subsequently face with registry engagement, questionable data validity and quality, and the inability to analyze registry data to population health- and practice-level quality improvement. Learn the root causes of these challenges and the options for overcoming them—without having to “redo” your registry.

Length: 58 min

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Are you tired of hearing all fluff and no substance on the topic of QCDR reporting? Are you in need of practical advice? Dr. Richardson has successfully guided several organizations through the entire registry reporting process. Webinar topics include quality measure selection tips, data collection methods, strategies to improve clinician engagement, and validation of registry reports.

Length 60 min

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Confused about MACRA, MIPS, and the QCDR? Need tips for successful registry reporting under the new Quality Payment Program? Join us and guest speaker Dr. Emily Richardson, a nationally-recognized expert in federal quality reporting programs and QCDRs.

Length: 49 min

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MIPS and other incentive payment systems have captured the attention of registry stewards. But you can’t lose sight of the three essential pillars to building a successful healthcare registry program. Prometheus’s approach, developed with a combination of healthcare informatics expertise and clinical data registry experience, empowers registry stewards to create QCDRs that meet the evolving needs of their organizations while staying relevant to their members.

Length: 49 min

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Our guest speaker, notable clinical informaticist Dr. Aziz Boxwala, CEO of Meliorix Inc., reviews the landscape of health information interoperability standards, focusing in particular on the FHIR specification from Health Level Seven.

Length: 45 min

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Proposed changes to the Common Rule are a rational liberalization of the rules for reusing research data and biospecimens. Learn how anticipated regulations will impact clinical research and the steps you should be taking now to prepare your research infrastructure for success.

Length: 56 min

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Clinic and Research should enjoy a symbiotic relationship, but all too often lack the technical resources and governance processes to achieve true integration. Learn how to implement both a short- and long-term strategy for bridging the divide, including 5 concrete changes you can make today to improve data reuse.

Length: 50 min

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Learn why the best practice for exploring clinical research data across multiple studies and data types is to leverage “data marts.” Research centers and multi-site research networks are using these specialized tools to securely access permittable data faster than traditional query interfaces.

Length: 45 min

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A new standard promises to reduce the costs and improve the quality of multi-site data collection initiatives while simultaneously alleviating the burden on data providers. The NIH-funded, freely-available standard and set of conversion tools facilitates the exchange, reuse, and storage of EDC configuration for REDCap, Qualtrics, and RexDB-based systems.

Length: 52 min

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Understand how to get started planning for a Data Request Portal (DRP), including prerequisites, challenges, and revenue models to consider prior to implementation. In Part 1 of this two-part series, we use a real-world case-study to introduce the opportunities and challenges of sharing clinical registry data.

Length: 1 hr

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Implementing a Data Request Portal (DRP) requires intense scrutiny of clinical registry data up-front. Learn how to properly evaluate and describe your data for use in a DRP or other data sharing process, what it looks like to use a DRP, and how to measure the impact and productivity of the data you make available.

Length: 28 min

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Open source tools aimed at improving health-related research, such as Apple’s ResearchKit, are growing in number and popularity. These tools have the potential to accelerate software delivery timelines, reduce costs, and spur innovation. But they also create risks that an educated consumer of clinical research software should know how to recognize and manage. Learn how.

Length: 1 hr

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Health-oriented open source (OS) tools are growing in number and popularity.  Expand your understanding of the opportunities and risks of using OS tools by learning how to: (1) resolve conflicts around ownership of data and relevant works, (2) evaluate OS projects for maintainability, and (3) review OS business models for sustainability.

Length: 52 min

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