The Clinical Problem Solvers

JUNE 26, 2023

Episode Learning Objectives After listening to this episode, learners will be able to… Differentiate between stigma and bias in health care and the electronic health record using provided examples. Describe difficulties and examples of how to measure unconscious race bias in medical practice.

Electronics 52

Electronics Internal Medicine Patient-Centered Healthcare 52

FDA Law

MARCH 8, 2023

By Véronique Li, Senior Medical Device Regulation Expert — On March 17, 2023, enhancements to FDA’s electronic Medical Device Reporting (eMDR) system will go live. Manufacturers who submit reports via the FDA Electronic Submissions Gateway are being advised to update their systems by this time.

Electronics 59

Electronics Manufacturing Provider Medical 59

33 Charts

OCTOBER 2, 2021

The zero-sum medical day In many healthcare systems the Epic feature is turned on and health professionals are expected to respond. The problem is that doctors work in what I call a zero-sum medical day. While this may help the zero-sum medical day on one level, compensation models don’t necessarily fix the problem of human bandwidth.

Patients 75

Patients IT Provider Family Doctor 75

GeriPal

MAY 18, 2023

Summary Transcript Summary Hot off the press is a brand spanking new updated 2023 AGS Beers Criteria for Potentially Inappropriate Medication Use in Older Adults. The Beers Criteria is one of the most frequently cited reference tools in geriatrics, detailing potentially inappropriate medications to prescribe to older people.

Medical 97

Medical IT Patients Clinic 97

GeriPal

JUNE 19, 2025

Noelle Marie 01:24 I think it really speaks a lot to my own personal journey and I’m pretty sure a lot of trans and gender diverse individuals also resonate with and it really speaks about our transition, celebrating our authentic selves, how society views us and how we view ourselves when we stand in front of a mirror.

Individual 81

Individual Community IT Chronic Condition 81

FDA Law

DECEMBER 18, 2022

Mullen — On December 9, 2022, FDA issued a draft guidance document on the Voluntary Malfunction Summary Reporting (VMSR) Program for medical devices. FDA began an initial VMSR pilot program in 2015. Summary malfunction reports should be submitted electronically on Form FDA 3500A.

Medical 59

Medical Manufacturing Individual Provider 59

GeriPal

DECEMBER 8, 2022

Integration of Person-Centered Narratives Into the Electronic Health Record: Study Protocol. Connection — The Integration of a Person-Centered Narrative Intervention into the Electronic Health Record : An implementation study. Bennett, C.R., What Mattered Then, Now, and Always: Illness Narratives From Persons of Color.

Patient-Centered 115

Patient-Centered Illness Healthcare IT 115