Summary Basis News Today

As we take a breather during the holiday whirlwind, we wanted to flag for readers a recent development in advertising and promotion regulation that FDA quietly released nearly a month ago.

Under Food Drug and Cosmetic Act, FDA may authorize unapproved medical products, including drugs, for use in an emergency to diagnose diseases COVID. FDA’s review process abbreviated and requirements for obtaining EUA less burdensome than for obtaining full FDA approval.

As we take a breather during the holiday whirlwind, we wanted to flag for readers a recent development in advertising and promotion regulation that FDA quietly released nearly a month...

A document used by the U.S. Food and Drug Administration (FDA) to approve Moderna's Wuhan coronavirus (Covid-19) mRNA (messenger RNA) "vaccine" has been scrubbed from the internet [...]

The Food and Drug Administration (FDA) has restored a document outlining why it approved Moderna's COVID-19 vaccine, days ...

Included references to unpublished analysis that found rates of post-vaccination heart inflammation were higher than any U.S. agency had found before!

The best uncensored news, information, and analysis.

ZeroHedge - On a long enough timeline, the survival rate for everyone drops to zero

A Food and Drug Administration (FDA) document explaining why the agency approved Moderna's COVID-19 vaccine was removed from ...

Generic drug names are often long, but they can tell doctors what type of medicine it is and how it works. But it’s brand names that appear first and most prominently in Health Canada materials.