Of course they are going to approve it....without it few people will take the booster sending everyone back to square one...this has all been coordinated by Dr Falsi...a week ago he said ‘he hoped the FDA would approve it by the end of the month.’
And here it is...
""On 18 August, before the news that the FDA would not be holding a formal committee meeting, the president of the Infectious Diseases Society of America Barbara Alexander praised the impact of the VRBPAC meetings as “a critical and necessary part” of the process for assessing whether to give booster doses.6""
There is no legitimate reason to push this hard for something that is 99.8% survivable.
The agenda here is NOT public Health and Safety.
.