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Medicinal cannabis: Why more clinical trials and better access is needed

Drug Discovery World

There are more than 1300 clinical trials on cannabis underway and companies focused on the cultivation and manufacturing of cannabis are also educating doctors and patients about its potential pharmaceutical use. Germany only has three licenses, and the current facilities are a small fraction of total sales.

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Article FDA Thank You FDA gives companies leeway to go after misinformation, but not free reign

Agency IQ

those sold under authorization from a licensed provider or other regulatory-specific situations) and is submitted as part of the medical device’s listing (general controls), and the agency may request a copy of all advertising materials for good cause ( See a Congressional Research Service explainer on this topic here ).

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Healthcare, HIPAA, Sitecore and BAAs

Perficient: Drug Development

The other part of the definition is what constitutes “health information.” As a matter of fact, if a client has a license to the full versions of Sitecore Personalize and CDP they can use the same conditions and segments they define in Personalize as XM Cloud personalization rules.

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Ceracare

The Pharma Data

Definitely not! Because it was engineered based on teachings from one of the longest living doctors in the world, Ceracare formula is. conditions you may have, please contact your doctor. offered by a physician or other licensed healthcare provider. Improves energetic well-being, combating fatigue and increasing vitality.

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Unity

The Pharma Data

Definitely not! Because it was engineered based on teachings from one of the longest living doctors in the world, Unity formula is. conditions you may have, please contact your doctor. offered by a physician or other licensed healthcare provider. Powerful anti-oxidants ingredients that help to support a healthy heart*.

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A Question 30 Years in the Making: Would a Final LDT Rule Withstand Judicial Scrutiny?

FDA Law Blog: Biosimilars

The PR goes on to state that the FD&C Act definition of a device does not turn on where or by whom a test system is “manufactured.” FDA recognizes that the FD&C Act exempts licensed healthcare practitioners from certain device regulations if they manufacture devices solely for use in the course of their professional practice.

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Where's the Synthetic Blood?

Codon

While blood doesn’t fit neatly into the various definitions of an organ , it still comprises a discrete system with specific functions. It is licensed in Russia and South Africa and is included in a few compassionate use programs across the globe, meaning it can be used clinically in cases where patients have few remaining options.