Compliancy Group

MARCH 25, 2024

In today’s complex healthcare landscape, compliance is crucial. A healthcare compliance due diligence checklist is one essential tool that can help organizations in their quest for compliance. What is a Healthcare Compliance Due Diligence Checklist? What is a Healthcare Compliance Due Diligence Checklist?

Due Diligence 40

Due Diligence Compliance Informed Consent Fraud 40

AIHC

SEPTEMBER 5, 2023

Compliance Considerations for Best Outcomes Written in collaboration with the AIHC Volunteer Education Committee Delivering mental health services via telehealth has increased since the COVID-19 pandemic. Obtaining informed consent with your patient is typically done before the first appointment.

COVID-19 59

COVID-19 Telemedicine Informed Consent Compliance 59

Healthcare Law Today

DECEMBER 12, 2022

He advises entrepreneurial health care providers and technology companies on business arrangements, compliance, and corporate matters in telemedicine, digital health, remote patient monitoring, and click-and-mortar services. I’m currently Deputy General Counsel of LifeMD, a growing telemedicine company.

Telemedicine 49

Telemedicine Fraud Governance Compliance 49

Hall Render

SEPTEMBER 14, 2023

For health care institutions conducting DCTs, considerations include compliance with fraud and abuse and beneficiary inducement requirements. Practical Takeaways Sponsors should evaluate how to ensure DCT participants have access to any necessary digital health technology.

FDA 40

FDA Informed Consent COVID-19 Fraud 40

HIPAA Journal

JANUARY 16, 2023

AI is used by the finance industry to detect potential credit card fraud. Although specific concerns differ by organization, the concerns can generally be categorized as informed consent to use data, safety and transparency, algorithmic fairness, and data privacy. .

Governance 64

Governance HIPAA World Health Informed Consent 64

C&M Health Law

JUNE 15, 2021

This article was originally published in Corporate Compliance Insights. bribery, fraud, misuse). Suppose that a biopharmaceutical enterprise submits regulatory approval for a new product, only to realize that the data collected from outsourced clinical trials is based on insufficiently informed consent.

Due Diligence 40

Due Diligence Licensing Informed Consent HIPAA 40

Drug & Device Law

DECEMBER 29, 2023

2023) ( Buckman preemption barred MDL asserting fraud on EPA), cert. Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Negligence requires an evaluation of a defendant’s reasonableness, and all relevant NC authority includes relevant regulatory compliance in that mix. 4th 696 (3d.

FDA 105

FDA US Department of Health and Human Services COVID-19 COVID-19 Vaccine 105

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. has no power to enforce compliance”), aff’d , 405 F. 23 in its current form. Smith, LLC , 2010 WL 11566367, at *7 (N.D.

Doctors 52

Doctors Fraud Licensing Compliance 52