Bill of Health
FEBRUARY 12, 2024
What about informed consent and other ethical issues? While the current informed consent form used by facilitators does address some aspects of concern ( like the use of touch , 333-333-5040 (9) ), it does not address other aspects like suggestibility or power dynamics within the facilitator/client relationship.
MedTrainer
NOVEMBER 5, 2023
This article provides an overview of key factors you’ll want to know about healthcare compliance in Washington. The Colorado Medical Board enforces the licensing standards for Medical Doctors (M.D.s), Doctors of Osteopathy (D.O.s), Physician Assistants (P.A.s), and Anesthesiology Assistants (A.A.s).
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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.
Bill of Health
MARCH 9, 2022
The phenomenon of citing anecdotal evidence as if it is scientific evidence appears across training materials, research articles, and general discussions by stakeholders (e.g., Mithoefer & Haden ).
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.
Medisys Compliance
APRIL 11, 2022
In this article, we shared list of required documents for ambulatory surgery centers who are beneficiaries of Medicare. Informed consent. Documentation of the name of the licensed independent practitioner responsible for the discharge. Documentation of vital signs, assessments, and other findings. Nurses’ notes.
C&M Health Law
JUNE 15, 2021
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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