Remove 2017 Remove Informed consent Remove Presentation
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5 Risk Control Considerations as Nurse Practitioners’ Scope of Practice Expands

Minority Nurse

increase compared to the average total incurred in the 2017 dataset ($300,506). of claims in 2017 to 37.1% Informed Consent. Informed consent is a cornerstone of ethical medical practice, and NPs must ensure that they obtain consent appropriately before performing procedures or prescribing treatments.

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Undisclosed Conflicts of Interest by Physicians Creating the CDC Opioid Prescribing Guidelines: Bad Faith or Incompetence?

Pallimed

WLF’s complaint compelled the CDC to re-open a second open comment period for the public, lasting 30 days in duration, rather than the two-day period for comment which CDC had originally presented via a September 2015 webinar (4, 35). Presented on February 10, 2022, for the Annual Assembly of Hospice and Palliative Care (Virtual Conference).

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Analysis of U.S. Food and Drug Administration Draft Guidance on Clinical Trials with Psychedelic Drugs

Healthcare Law Insights blog

FDA recommends referring to its 2017 guidance “Assessment of Abuse Potential of Drugs” for details. Clinical FDA believes that the characteristics of psychedelic drugs present challenges in designing adequate and well-controlled (AWC) clinical studies. For one, the use of an inert placebo may present a challenge.