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Philip Haddad's avatar

Wonderful article, and thank you so much for defending our health on the global stage!

Big props to you, Sayer, and Scott - National Health Federation!

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Lionel Serrane's avatar

Transparency and Adverse Event Monitoring :

Question: How can U.N and FDA staff improve the current system of adverse event reporting and monitoring for supplements while ensuring an increased sense of transparency in the regulatory process for the general public? Safety Standards

The discussion of safety standards reflects actual regulatory frameworks:

In the US, supplements don't require pre-market approval under DSHEA

https://pmc.ncbi.nlm.nih.gov/articles/PMC6513729/#:~:text=The%20U.S.%20Dietary%20Supplement,DSHEA%20outlined%20the%20legal

Manufacturers are responsible for ensuring safety before marketing

https://www.fda.gov/food/dietary-supplements#:~:text=FDA%20has%20the%20authority,after%20it%20reaches%20the

Post-market surveillance is conducted by regulatory authorities

https://www.fda.gov/food/dietary-supplements#:~:text=Manufacturers%20and%20distributors%20of,responsible%20for%20evaluating%20the

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