Annals of Family Medicine

NOVEMBER 20, 2024

Objective: To validate and apply electronic medical record (EMR)-based definitions for mood and anxiety disorders (inc. Algorithms to capture these conditions together produced stronger agreement compared to individual definitions. depression, anxiety, bipolar disorder), and schizophrenia.

Primary Care 130

Primary Care Electronics Medical Mental Health 130

Physician's Weekly

JUNE 28, 2025

Studies were included if they assessed the prevalence of long-term neurological symptoms in individuals who had recovered from COVID-19 and had a follow-up duration of at least 6 months.

Mental Health 75

Mental Health Electronics Individual Clinic 75

Integrated Care News by CFHA

MAY 19, 2025

This position statement is intended to clarify and inform all members, partners, and the public regarding CFHA’s organizational stance on MBC. MBC is a clinical process that includes repeated measurement to monitor treatment progress and to inform collaborative treatment planning over the course of care. (1) What is MBC? 1, 8, 9) d.

Integrated Care 100

Integrated Care Mental Health Healthcare Clinical Practice 100

Annals of Family Medicine

NOVEMBER 20, 2024

Context Administrative activities, including work related to caring for individual patients and clinic administration, may play a substantial role in understanding changes to primary care workload. Results/Findings Information management is central to health care delivery, but often not valued or actively supported.

Primary Care 130

Primary Care Management Nurse Practitioner Family Physician 130

ABIM

MARCH 27, 2025

For more information, register for an informational webinar that will take place on April 15 at 6 p.m. The grant may be applied to an existing research project with a new scope or an original research project. Applications to the ABMS Visiting Scholars Program are open now through June 23, 2025.

Board-Certified 52

Board-Certified Medical Specialty Internal Medicine Education 52

Annals of Family Medicine

NOVEMBER 20, 2024

Results: Based on the electronic databases (Medline, Embase, CINAHL) search and the reference list of key studies, from 2967 studies, 30 were eligible for the final review. Only 4 indicators directly capture the individual contribution of IPC providers.

Primary Care 130

Primary Care Electronics Individual Provider 130

Annals of Family Medicine

NOVEMBER 20, 2024

A proportion of these ADEs can be explained by a difference in enzyme activity between individuals. Intra-individual variation in genetic composition is one of the key contributing factors determining enzyme activity. Context Ten percent of patients using prescription drugs experience adverse drug events (ADE).

Primary Care 130

Primary Care Education Family Medicine DO 130

Annals of Family Medicine

NOVEMBER 20, 2024

This analysis was part of a larger implementation study called PATHWEIGH, which provides a toolset embedded in the EpicTM electronic health record and other supportive services to help practices provide weight management to their patients. Study Design and Analysis: Qualitative study involving key informant interviews over two years.

Primary Care 130

Primary Care Electronics Provider Management 130

FDA Law Blog

JULY 31, 2023

Practitioner’s Partial Fill Request A practitioner issuing a schedule II prescription who wants it to be partially filled must specify the quantity to be dispensed in each partial filling on the face of a written prescription, in the written record of an emergency oral prescription, or in the record of an electronic prescription. b)(5)(i)).

Electronics 98

Electronics Consulting Patients Medical 98

The Motivated MD

OCTOBER 10, 2024

How, then, can any physician find the time to research individual companies and make educated decisions on which publicly traded businesses are undervalued? Instead of investing in individual stocks, why not buy all the most economically impactful stocks in a proportion that reflects an index of the market? We simply cannot.

Finance 52

Finance Individual Management IT 52

BMJ

AUGUST 20, 2021

In its best use case, such technology would provide the foundation of person-level digital information systems that can be used to accurately collect and use data in at two critical levels: in real-time to improve individual patient outcomes, and aggregated to monitor the health status of a population, i.e. the big numbers.

Patient-Centered 40

Patient-Centered Clinic Provider Patients 40

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. b)(1)(iii).

Electronics 59

Electronics Manufacturing Provider Medical 59

The Motivated MD

DECEMBER 18, 2024

However, I think it is important to highlight some of the more frequent offenders to describe how this commonly affects individuals’ lives. Though this is in no way an exhaustive list, the following represents what I believe to be the most common culprits of lifestyle creep and financial pressures in individuals’ lives.

Finance 52

Finance Insurance Individual IT 52

FDA Law Blog

APRIL 19, 2022

Houck — Effective May 11, 2022, the Drug Enforcement Administration (“DEA”) will require all applications and renewals for registration to be submitted electronically. DEA noted that the National Association of Chain Drug Stores (“NACDS”) and three other individuals commented on the proposed rule. By Larry K. 1,030 (Jan.

Electronics 75

Electronics Individual IT 75

Aspiring Minority Doctor

APRIL 18, 2021

There is also the option of electronic health record (EHR) training and support work where you would travel to various hospitals/clinics around the country and train individuals on how to use EMR systems. This would require relocating and I am not aware of how much it pays.

GP 52

GP Medical Student Insurance General Practitioner 52

FDA Law Blog

FEBRUARY 9, 2024

is used in a clinical investigation of a drug or biologic under IND and the DHT meets the definition of a significant risk device a submission of an IDE to the FDA is required unless all the information required for the IDE is contained in the IND. smartphones and tablets) for remote data acquisition in a clinical investigation.

Clinic 105

Clinic Manufacturing Provider Electronics 105

Permanente Medicine

MAY 20, 2025

Contributing to this challenge is the exponential growth of information, an expanding population of older adults, and office visit documentation. Information is coming at clinicians, whether they be doctors, nurses, pharmacists, faster than ever, and there is a transparency that exists around us.

Patient-Centered 52

Patient-Centered Patients Medical IT 52

The Motivated MD

NOVEMBER 26, 2024

The decision to rent or buy a home is the root of much anxiety in many individuals’ lives. I overhear individuals say things like ‘owning a home is the best investment you can make,’ and’ if you are renting, you are just ‘throwing your money away.’ As always… Stay motivated! The Motivated M.D.

Finance 52

Finance Insurance Individual Medical Advice 52

33 Charts

OCTOBER 2, 2021

Medicine is facing a crisis of information. Beyond the increase of biomedical information are rising demands for physician response to portal messaging (MyChart messages) and review of wearable generated data. And in my experience the exchange of information from the Cures Act Final Rule has added new dialog around test results.

Patients 75

Patients IT Provider Family Doctor 75

FDA Law Blog

MARCH 7, 2024

FDA notes that the distinctions between responsibilities for these groups and DMCs should be clearly defined, particularly with respect to access to unblinded information. FDA has dropped such restrictive language in the new draft guidance, and instead intends to refer “relevant and important” information.

Clinic 105

Clinic Provider IT Utilities 105

FDA Law Blog

JULY 10, 2023

After a firm submits a 510(k) to FDA, FDA will request still more information after a first-pass review. According to the 2 nd Quarter FY2023 MDUFA V Performance Report , FDA issued a request for additional information (AI request) on the first FDA review cycle for 63% to 68% of 510(k)s submitted in FY2018 to FY2022.

Provider 75

Provider IT Engineering Medical 75

FDA Law Blog

JUNE 21, 2023

enable individuals to have virtual consultations with healthcare providers through video calls or online platforms), at-home diagnostics (e.g., enable individuals to have virtual consultations with healthcare providers through video calls or online platforms), at-home diagnostics (e.g., telemedicine and telehealth solutions (e.g.,

Medical 45

Medical Patients Healthcare Electronics 45

FDA Law Blog

MAY 4, 2023

DCTs often include the use of digital health technologies (DHTs), which is technology that can be used to remotely capture and transmit health care information. For example, the draft guidance notes that the trial’s data management plan should include information about the multiple sources of data collection.

Clinic 59

Clinic Telehealth Provider Electronics 59

FDA Law Blog

MAY 20, 2021

The investigators ask the registrant’s designated responsible employee, such as the Operations or Compliance Manager, for informed consent by signing a Notice of Inspection (“DEA Form-82”). Registrants should consult with counsel and their Human Resources departments in deciding whether to provide this information.

Management 40

Management Consulting Provider Physicals 40

FDA Law Blog

MAY 20, 2021

The investigators ask the registrant’s designated responsible employee, such as the Operations or Compliance Manager, for informed consent by signing a Notice of Inspection (“DEA Form-82”). Registrants should consult with counsel and their Human Resources departments in deciding whether to provide this information.

Management 40

Management Consulting Provider Physicals 40

GeriPal

JULY 19, 2024

What should we use to screen individuals? I heard this beautiful thing the other day, which was to an electronic medical record, I am not a whole person. And either of those could be given to the patient or an informant. Who should get it if anyone? What happens after they test positive? And we give a variety of validated tools.

Screening 119

Screening Primary Care Patient-Centered IT 119

Annals of Family Medicine

NOVEMBER 20, 2024

Methods: In-depth semi-structured interviews using the Database of Individual Patient Experiences (DIPEx) methodology. Participants were recruited via electronic healthcare records, community tabling events, and social media efforts. Cancer Prevention: Little to no awareness or information about cervical cancer.

Diagnosis 130

Diagnosis Screening Transportation Diagnose 130

Permanente Medicine

JUNE 3, 2025

I just listened to the one on national cancer care that we’re doing, which was very informative and pretty impressive. I think sometimes we don’t necessarily realize the importance in the role that each of us individually as physicians can have with patients both within the exam room but also globally.

IT 52

IT Patient-Centered Patients Medical 52

Medical Xpress

JUNE 16, 2025

More information: ScienceDirect has more on ibogaine. Journal information: Nature Medicine © 2025 HealthDay. The content is provided for information purposes only. However, we do not guarantee individual replies due to the high volume of messages. All rights reserved. Your feedback is important to us.

Mental Health 52

Mental Health IT Medical Specialization 52

Medical Xpress

JUNE 16, 2025

In a study published in Nature Communications , led by researchers at National Taiwan University (NTU) and National Tsing Hua University (NTHU), scientists used the deepest-ever two-photon calcium imaging in awake mice to directly observe how individual SCN neurons respond to light. The content is provided for information purposes only.

Provider 109

Provider Medical Complication Diabetes 109

The Motivated MD

SEPTEMBER 19, 2024

For the better half of 2024, I have been periodically writing posts that are individual articles that double as potential chapters to a future book. Before we discuss each individual savings account, let us first highlight exactly what it means to ‘automate’ your savings. Saving money is simple but not easy.

Finance 52

Finance Education Individual Healthcare Professional 52

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. 1310.06. .

Government 116

Government Electronics Education Individual 116

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 85

Individual Community IT Chronic Condition 85

The Clinical Problem Solvers

DECEMBER 20, 2021

Fields Guests: Thu Quach, PhD, and Tung Nguyen, MD Time Stamps 00:00 Introduction 04:00 How Dr. Thu Quach’s and Dr. Tung Nguyen’s journeys shape their work 11:40 Policy work as a way of mitigating burnout 12:55 Balancing individual and communal focus (include?) Insufficient language services (i.e.,

Community 52

Community Patient-Centered Relationship Healthcare 52

FDA Law Blog

JULY 7, 2024

However, the guidance provides no new information on how FDA expects laboratories to implement these new requirements. To be sure, Table 2 provides a handy visual of the categories of LDTs, the timeline for phaseout, and the scope of enforcement discretion for each test category. report certain device malfunctions, and.

Manufacturing 64

Manufacturing Provider Physicals Electronics 64

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. Summary malfunction reports should be submitted electronically on Form FDA 3500A.

Medical 59

Medical Manufacturing Individual Provider 59

GeriPal

JULY 21, 2022

That’s where it really gets to this individual risks and balances, individual situation. So just starting to unpack what’s happening in an individual’s life can maybe then lead to more conversations and assessment. I can get you guys that information. Alex: Yeah.

Families 102

Families Family IT Diagnosis 102