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What is Healthcare Compliance Ethics?

MedTrainer

That’s why healthcare compliance regulations exist. What is healthcare compliance ethics? In this blog, we’ll discuss how compliance came into being and why ethics are closely monitored by federal, state, and local governments. What is Healthcare Compliance Ethics? Who Enforces Healthcare Compliance Ethics?

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Orientation to the Operating Room for Sales Professionals

American Medical Compliance

Languages: American English Key features: Audio narration, learning activity, and post-assessment Get Certified American Medical Compliance (AMC) is a leader in the industry for compliance, Billing, and HR solutions. To become certified, please visit us at American Medical Compliance (AMC).

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Introduction to Telebehavioral Health

AIHC

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. However, they would share information and processes essential to these providers’ licensure and regulations.

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Telehealth for Behavioral Healthcare

Verisys

For example, waivers were put into place temporarily lifting the requirement that providers be licensed in the states that they provide telehealth services (see below). These license verification requirements have continued to change, so keeping up with regulations in telehealth is vital to compliance. Written by Verisys.

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Is Your Data Supply Chain Ethical? Don’t Restrict Due Diligence to Physical Operations.

C&M Health Law

This article was originally published in Corporate Compliance Insights. Health Insurance Portability and Accountability Act (HIPAA) can present several areas of exposure. Both your company’s data supply chain and its physical version have fundamentally similar business risks.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

Eudralex, Volume 4: GMP Guidelines and Annexes Revision of the EU GMP Guide Annex 11 “Computerized Systems” – Presentation of Concept Paper, 18 November 2022 On 16 November 2022, the European Medicines Agency EMA published a concept paper on the planned revision of Annex 11 “Computerized Systems.”

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The BFDs – The Ten Best Prescription Drug/Medical Device Decisions of 2023

Drug & Device Law

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. Plaintiffs’ own litigation strategy thus opened the door to compliance evidence.

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