Integrated Care News by CFHA
MAY 19, 2025
The full process of MBC (Collect, Share, and Act) supports a shared decision-making framework that is inherently therapeutic, with the aim of improving treatment outcomes as well as promoting the overall wellness of individuals and populations. (2, 1, 8, 9) d. Artificial Intelligence), etc. American Psychological Association.
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. Identify strategies to mitigate bias and stigma in the electronic health record as a trainee and medical practitioner.
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FDA Law Blog
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.
33 Charts
OCTOBER 2, 2021
And individual practice styles are fine. This thread from a 2015 post illustrates how varying needs of a child with ulcerative colitis call for different ways to connect: Take Luke, a school-aged child with moderate ulcerative colitis complicated by sclerosing cholangitis. It’s everything written here about electronic health records.
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.
FDA Law Blog
FEBRUARY 7, 2024
Gilbert — Last week, DEA and DOJ announced a $59 million civil penalty settlement with eBay related to the failure to comply with Controlled Substances Act (CSA) requirements for identifying purchasers, maintaining records, and filing reports of individuals selling/purchasing pill presses and encapsulating machines.
FDA Law Blog
DECEMBER 18, 2022
Generally, FDA’s MDR regulations require device manufacturers to submit Medical Device Reports (MDRs) for individual reportable malfunctions within 30 calendar days of the manufacturer becoming aware of the malfunction. FDA began an initial VMSR pilot program in 2015. In that letter, FDA stated that it would “permit manufacturers.
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