AIHC

SEPTEMBER 5, 2023

In many states, the definition of telemedicine and/or telehealth stipulates that the delivery of services must occur in “real time,” automatically excluding store-and-forward as a part of telemedicine and/or telehealth altogether. Obtaining informed consent with your patient is typically done before the first appointment.

Telemedicine 59

Telemedicine COVID-19 Compliance Informed Consent 59

Healthcare Law Today

DECEMBER 12, 2022

Maureen has extensive experience handling malicious insider matters ranging from employee fraud, embezzlement, and misappropriation to breaches of non-solicitation, non-compete and confidentiality agreements. I’m currently Deputy General Counsel of LifeMD, a growing telemedicine company. Maureen Stewart.

Telemedicine 49

Telemedicine Fraud Governance Compliance 49

HIPAA Journal

JANUARY 16, 2023

One of the reasons why some people approach the topic of AI in healthcare with a degree of apprehension is that different sources offer different definitions of AI. To quote Microsoft´s definitions of the two terms: . AI is used by the finance industry to detect potential credit card fraud.

Governance 65

Governance HIPAA World Health Informed Consent 65

Drug & Device Law

DECEMBER 21, 2023

The logic of the consumer fraud claim made no sense. Allegedly, consumers deprived of efficacy (not risk) information had their informed consent rights infringed, which in the case of persons without the genetic difference, meant that they were spared the expense of undergoing negative genetic testing.

FDA 52

FDA Fraud Informed Consent 52

Drug & Device Law

AUGUST 8, 2022

Anyway, this fraudulent “doctor” allegedly “touched them without informed consent” and caused them “emotional distress. The unfortunate truth is that ECFMG was also a victim of this fake doctor’s fraud. Typically overblown MDL claims for “fraud” and “conspiracy” also failed. 23 in its current form.

Doctors 52

Doctors Fraud Licensing Compliance 52

Drug & Device Law

NOVEMBER 28, 2022

Moline obtained from her employer’s institutional review board to conduct the article was structured to “reference[] federal regulations governing human subject research,” while simultaneously “waiv[ing] the requirement that Dr. Moline obtain informed consent from the individuals whose cases she planned to study.”

Informed Consent 59

Informed Consent Fraud FDA HIPAA 59