Blog Electronics Individual Medical 
A Country Doctor Writes
JUNE 8, 2025
It’s been six years since I posted this on my WordPress blog and the reaction has been an almost deafening silence. In many ways, EMR office notes are created so automatically and by more than one individual, that the author’s (clinician’s) logic can be elusive when you read the note.
Integrated Care News by CFHA
MAY 8, 2025
WHO grouped these determinants into contextual, individual, and group influences and vaccine/vaccination-specific issues. I discussed this debate in my previous blog post. And yet others pose the question, “On what basis should we judge whether a parent’s medical decision for their child is morally acceptable?”.
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ABIM
MARCH 27, 2025
To help advance this mission, ABIM and the ABIM Foundation are proud to sponsor the American Board of Medical Specialties (ABMS) Visiting Scholars Program , a year-long, part-time research program that supports early career physicians and researchers as they strive to become leaders in their field.
FDA Law Blog
JULY 12, 2022
Mullen — Last month, FDA announced two important steps towards accepting electronic 510(k) submissions. On June 30, individuals with access to the CCP (i.e., While the tool is useful for ensuring the proper electronic formatting for a 510(k) submission, the output still needed to be downloaded and sent to FDA. By Allyson B.
FDA Law Blog
JULY 31, 2023
In addition, a pharmacist could partially fill a schedule II prescription issued to patients in a Long Term Care Facility or who have a terminal medical illness diagnosis. 21 U.S.C. § The Final Rule a. Patient Request A patient may also request that their prescription for a schedule II substance be partially filled.
FDA Law Blog
DECEMBER 4, 2023
Pharmacists’ Corresponding Responsibility A controlled substance prescription, to be valid, must be issued for “a legitimate medical purpose by an individual practitioner acting in the usual course of [their] professional practice.” Zarzamora Press Release. The government asserted additional allegations that are outside our scope.
FDA Law Blog
FEBRUARY 9, 2024
Lenz, Principal Medical Device Regulation Expert & Lisa M. Baumhardt, Senior Medical Device Regulation Expert — As an end of the year gift, FDA finalized its guidance document, Digital Health Technologies for Remote Data Acquisition in Clinical Investigations , in late December. By Adrienne R.
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