Seems the GMO therapies known as “COVID vaccines” are likely to need \boosters\ in the future.
Kinda like the flu...
Will these boosters need a new Emergency Use Authorization or will we just have un-ending, continuous EUAs for The COOF?
Small changes to an existing vaccine or medicine require a specific testing and re-authorization process. The Influenza vaccines go through this each year. In essence, you have to demonstrate that the changes made are minor (no change to the delivery or function, just a minor tweak to the antigen) and submit a license supplement with all the data around what changes you’re making.
If you’re using a live attenuated version of the pathogen in the vaccine, you must conduct a small clinical study to demonstrate that the attenuation process is working. If you’re not using a live pathogen, no additional clinical trials are typically required.