Annals of Family Medicine
NOVEMBER 20, 2024
Context: Mental health conditions have increasing prevalence, co-occurrence, and high management burden within primary care settings. Population: 1,692,987 patients from seven Canadian provinces with a visit between January 1, 2011, and December 31, 2021. depression, anxiety, bipolar disorder), and schizophrenia. spec, 80.7,
Today's Hospitalist
MAY 9, 2025
For many of us, the emergence of medical scribes, both in-person and remote, provided a valuable solution, offloading documentation and allowing us to have more focused patient interactions. It can differentiate between a physician’s questions and a patient’s responses and even filter out non-relevant small talk.
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FDA Law Blog
MAY 3, 2021
Maintaining complete and accurate records with direct, ongoing oversight by management reduces risk of internal employee pilferage and maximizes potential for early detection should diversion occur. 39,318 , 39,324 (July 6, 2011). 6 (2011) (statement of Michele M. On Energy and Commerce, 112th Cong.
The Clinical Problem Solvers
DECEMBER 16, 2020
19:05 Clarifying the “ethics vs science” argument and critiquing research techniques 22:00 Resurgence of race-based speculation in COVID-19-related research 25:57 Implantation of ideas about innate racial inferiority within medicine 28:32 Will removal of race from algorithms potentially harm our patients?
FDA Law Blog
MAY 3, 2021
Maintaining complete and accurate records with direct, ongoing oversight by management reduces risk of internal employee pilferage and maximizes potential for early detection should diversion occur. 39,318 , 39,324 (July 6, 2011). 6 (2011) (statement of Michele M. On Energy and Commerce, 112th Cong.
FDA Law Blog
NOVEMBER 9, 2023
The FDA Food Safety Modernization Act (FSMA) enacted in 2011, aims to ensure the U.S. As a result FDA can make better informed decisions in managing potential risks of imported food into the United States. food supply is safe by shifting the focus of federal regulators from responding to contamination to preventing it.
FDA Law Blog
JANUARY 4, 2023
The Agency referred to its 2011 FDA Guidance for Industry: Potency Tests for Cellular and Gene Therapy Products during the town hall. Per the 2011 FDA Guidance, developers should validate the assay prior to conducting a clinical study that will investigate the efficacy for licensure. Comparability.
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