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Your Healthcare Compliance Due Diligence Checklist

Compliancy Group

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?

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Managing Healthcare Compliance in Colorado

MedTrainer

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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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. This article is not intended as legal or consulting advice. Telehealth rules and regulations vary greatly by state.

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List of Documents for Ambulatory Surgery Centers (ASCs)

Medisys Compliance

In this article, we shared list of required documents for ambulatory surgery centers who are beneficiaries of Medicare. Informed consent. Documentation of compliance with discharge criteria Condition of the patient on discharge. Documentation of vital signs, assessments, and other findings. Nurses’ notes.

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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. 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.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

The application/notification must be submitted via the EUDAMED database (Article 69 IVDR). It includes aspects such as home health visits, remote monitoring and diagnostics, direct-to-patient shipment of study drugs, and electronic informed consent.

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – Spring

SQA

China Regulatory Roundup: Latest Guidelines for Medical Device and IVD Compliance, 17 March 2022. The Points is an upgraded version of Practice for Cosmetics Production Licensing , implemented in 2016, with more stringent inspection requirements.

FDA 75