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Psychedelic medicines: are they gaining traction in Europe?

European Pharmaceutical Review

As psychedelics diffused into wider society and recreational use increased, some individuals reported…ongoing symptoms after the drugs had left the body” At a time when psychiatry lacked effective medical therapies, the discovery of LSD was of interest.

Medicine 114
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Healthcare Watch July/August 2022

PM360

Brand Beat: Juul Fights FDA Ban. Shortly after banning Juul from selling its products, the FDA placed a hold on its decision in order to review the company’s case more closely. however, the company is required to prove to the FDA that their e-cigarettes in fact benefit the public. appeals court in Washington, D.C.,

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Securing every dose with an edible security technology for safe medicines

European Pharmaceutical Review

The prevalence of fake drugs is a continually growing problem worldwide. Fake drugs can be categorised as substandard, falsified, counterfeit and diverted drugs, and the World Health Organization (WHO) broadly defines a counterfeit medicine as “one which is deliberately and fraudulently mislabelled with respect to identity and/or source.”

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Emerging Trends in Orthopedic Medical Device Industry

Medico Reach

Quite recently, the Food and Drug Administration (FDA) marked a historical moment when it approved Patient Specific Talus Spacer 3D-printed implants in 2021. Hence, there are obstacles like restrictive, albeit necessary, government regulations. This focus on advanced implants also extends to smart technology.

Medical 98
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Emerging Trends in Orthopedic Medical Device Industry

Medico Reach

Quite recently, the Food and Drug Administration (FDA) marked a historical moment when it approved Patient Specific Talus Spacer 3D-printed implants in 2021. Hence, there are obstacles like restrictive, albeit necessary, government regulations. This focus on advanced implants also extends to smart technology.

Medical 52
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The NIH on accelerating research using diverse biomedical datasets

pharmaphorum

Understanding these differences across diverse populations can help doctors and HCPs determine what medication and dosage best fit a patient. Food and Drug Administration (FDA). Martin is also the primary author of the pivotal FDA guidance document Collection of Race and Ethnicity Data in Clinical Trials.

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Uri Goren

Cadensee

It's become the main thing that the doctors are looking at now. And did you know at the time that you were a trailblazer in this space? It broke the confines of you being a doctor learning healthcare, learning to be a medical profession and that stayed there; it just broke it all. Interview Transcription (mild edits).