Bill of Health

JANUARY 29, 2024

In 2013, for instance, I published an essay titled “ A Declaration of Psychedelic Studies ,” which began with these words: “The scientific research community is in the midst of a ‘psychedelic renaissance,’ but sanctioned platforms for mainstream discussion are heavily weighted in the direction of objective scientific research.

Informed Consent 355

Informed Consent Bioethics Doctors 355

SQA

MAY 17, 2022

ANVISA’s RDC 665/2022 (link in Portuguese) replaces previous regulations, including RDC 16/2013 and IN 08/2013, and went into effect on 02 May 2022. Patients currently taking the products should consult with their doctor or healthcare provider about alternative treatment options.

FDA 75

FDA Compliance Informed Consent Hospitals 75

Drug & Device Law

JUNE 6, 2022

Further, “both doctors testified that they still prescribe [the drug] for patients with conditions similar to plaintiff’s condition.” 2013 WL 4516160, at *3 (N.M. 2013 WL 85291, at *8 (D.N.J. 2013) (no causation where prescribing physician “recommended that [plaintiff] restart [the drug] at the same dose and frequency. . .

FDA 59

FDA Doctors Malpractice Medical Personnel 59

Drug & Device Law

MAY 30, 2022

The law presumes that licensed doctors know what they are doing. 1978), where a hypertensive patient was injured after being injected with the defendant’s drug – despite warnings that “expressly directed the doctor administering the drug to refrain from giving it to a patient with hypertension.” 2013 WL 2457950, at *8 (N.D.

Doctors 59

Doctors Licensing Informed Consent Hospitals 59

Drug & Device Law

DECEMBER 29, 2023

Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Specifically, “it would be nonsensical to require directions for patient use for a drug that is injected into the patient by a doctor in a clinical setting.” The G/N MDL was created in 2013 and mostly settled in 2016.

FDA 105

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