MedTrainer

SEPTEMBER 20, 2023

Healthcare is a continuously evolving industry, especially when it comes to compliance. Compliance standards are consistently under scrutiny from regulatory organizations, which means healthcare professionals frequently need to refresh, re-train, and learn new concepts and best practices. What Is Microlearning?

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Compliance HIPAA Informed Consent Compliance Officers 98

MedTrainer

DECEMBER 7, 2023

State-specific governing bodies, such as the Bureau of Facility Standards , provide oversight with certain standards, adding a layer of complexity to successfully managing healthcare compliance in Idaho. Continue reading this overview for key aspects of healthcare compliance specific to the state of Idaho.

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Compliance Licensing Compliance Officers Informed Consent 52

MedTrainer

NOVEMBER 5, 2023

Colorado, like other states in the United States, has its own set of regulations and requirements that make managing healthcare compliance in Colorado tricky. To effectively manage compliance, healthcare organizations must establish a robust system for monitoring and interpreting these changes and swiftly implement necessary adjustments.

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Compliance Licensing Informed Consent Public Health 52

MedTrainer

OCTOBER 4, 2023

To ensure organizations meet these standards, federal healthcare compliance requirements have been put in place. Let’s look at some of the key federal healthcare compliance requirements, state-specific variations, and accreditation standards healthcare organizations must adhere to. What Are Federal Healthcare Compliance Requirements?

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Compliance Fraud HIPAA Governance 52

MedTrainer

OCTOBER 4, 2023

Corporate compliance training helps healthcare organizations balance the need to provide top-notch care with adhering to a plethora of regulations. What Is Corporate Compliance Training? What Is the Difference Between Corporate Compliance Training and Regulatory Compliance Training?

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Compliance Regulatory Compliance ADA Informed Consent 52

MedTrainer

APRIL 11, 2024

Incident reporting is essential to maintain a healthcare organization’s compliance with state and federal regulations and reveal what are the main types of healthcare incidents. MedTrainer offers all the functions listed above in an all-in-one compliance solution. There were 13 recalls during the same period in 2023. There were 45.9

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Compliance Informed Consent Malpractice Hospitals 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.

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FDA Informed Consent COVID-19 Fraud 40

AIHC

JANUARY 5, 2022

Think Again blog post related to the January 1, 2022, implementation of the Interim Final Rule (IFR) of the No Surprises Act. The American Medical Association (AMA) also posts helpful information for providers and offers an initial toolkit. Implement an efficient and compliant method of providing a good faith estimate.

Medical Billing 52

Medical Billing Health Insurance Hospitals Medicare 52

Bill of Health

FEBRUARY 29, 2024

Nepal’s National Parks and Wildlife Conservation Act does not include a provision for the free, prior, and informed consent of Indigenous Peoples as mandated by the Nepal-ratified United Nations Declaration on the Rights of Indigenous Peoples. Nor does the Forest Act 2019 contain provisions to protect the rights of Indigenous Peoples.

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Informed Consent Governance Compliance Public Health 201

SQA

FEBRUARY 15, 2023

It includes aspects such as home health visits, remote monitoring and diagnostics, direct-to-patient shipment of study drugs, and electronic informed consent. Decentralization is enabled by the advancement of digital tools, telemedicine, and more mobile and local healthcare.

US Department of Health and Human Services 40

US Department of Health and Human Services FDA COVID-19 World Health 40

SQA

MAY 17, 2022

China Regulatory Roundup: Latest Guidelines for Medical Device and IVD Compliance, 17 March 2022. For Investigator Sites, the subject areas are Organizational Aspects, Informed Consent of Trial Participants, Review of Trial Participant Data, and Management of Investigational Medicinal Product(s).

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FDA Compliance Informed Consent Hospitals 75

SQA

APRIL 30, 2021

generic, biosimilar, or hybrid application), informed consent is irrelevant provided that both applications relate to a medicinal product with the same qualitative and quantitative composition in active substances and the same pharmaceutical form. European Medicines Agency (EMA) – Biologics.

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COVID-19 Vaccine COVID-19 Compliance Governance 52

Drug & Device Law

DECEMBER 29, 2023

This year’s Drug & Device Law Blog top ten decisions of the year reinforced preemption – the most powerful defense we can assert. Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Plaintiffs’ own litigation strategy thus opened the door to compliance evidence. Strike one.

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

Drug & Device Law

JANUARY 28, 2022

Thanks to the Connecticut Supreme Court, blog readers can stop staring with guilt and/or determination at that copy of Moby Dick on the bookshelf and instead print a sprawling copy of Fajardo v. She sued the gynecologist, not the surgeon who implanted the mesh, for failing to obtain informed consent for the implant. at *13-*14.

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Informed Consent Malpractice Compliance 59

Drug & Device Law

APRIL 21, 2023

That would be especially true in states where regulatory compliance is a defense or partial defense. These paradigms are difficult to apply to healthcare providers, who operate under a different warnings regime that focused on informed consent. Try instructing a jury on how that ought to work.

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Informed Consent Malpractice FDA Regulatory Compliance 59