Compliancy Group

MARCH 25, 2024

A comprehensive due diligence checklist will cover areas such as licensing requirements, contractual agreements, fraud prevention measures, and risk management protocols. This article provides a general overview but does not constitute legal advice or an exhaustive list of all potential compliance considerations healthcare organizations face.

Due Diligence 52

Due Diligence Compliance Informed Consent Fraud 52

Hall Render

SEPTEMBER 14, 2023

For health care institutions conducting DCTs, considerations include compliance with fraud and abuse and beneficiary inducement requirements. Hall Render blog posts and articles are intended for informational purposes only.

FDA 40

FDA Informed Consent COVID-19 Fraud 40

AIHC

SEPTEMBER 5, 2023

This article is not intended as legal or consulting advice. If your practice is currently using a telebehavioral health approach for patient treatment, or if you organization is considering implementing this approach, we hope this article will give some food-for-thought on the topic.

COVID-19 59

COVID-19 Telemedicine Compliance Informed Consent 59

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

HIPAA Journal

JANUARY 16, 2023

This article aims to answer the questions what AI in healthcare is, what are – or what will be – the benefits of AI in healthcare, and how can concerns about the ethics of AI in healthcare be overcome. AI is used by the finance industry to detect potential credit card fraud.

Governance 67

Governance HIPAA World Health Informed Consent 67

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

DECEMBER 29, 2023

2023) (First Amendment bars state-law misrepresentation claims over “truth” of published scientific article) ( here ); National Association of Wheat Growers v. 2023) ( Buckman preemption barred MDL asserting fraud on EPA), cert. Plaintiff knew about it, too, since he signed an informed consent document mentioning it.

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