I am a retired PhD Clinical Microbiologist and worked for (at the time) Burroughs Wellcome LTD while going to grad school. The process of bringing a new drug or vaccine to market is a long one. These vaccines were rushed to market thanks to government induced hysteria without being adequately vetted. I will NEVER have any of them injected into my body, especially for a virus with a lower mortality than Flu A or B. I never bought into this covidiocy scamdemic from day one and was not the least bit reticent about expressing my opinion about it. I had it, and at 65 was supposedly part of the most at-risk demographic. To say the least I was underwhelmed. Granted I did not have any underlying medical conditions, which is the demographic that comprised the highest mortaligy demographic. I have had cases of Flu A that were far worse.
There are far too many galactically uninformed sheep in this country who take what they hear in our totally disingenuous "media" as truth.
Well you should understand the following:
Medical device/ pharmaceutical companies must test their products to present data to the FDA (for those that don’t know the FDA does not perform the tests).
You and your technicians find say, sterility failures. You want to go with a new packaging configuration.
Management doesn’t want to hear that.
You say “no, no, no, we’ve failed x number out of 1,000, it doesn’t meet inspection criteria”
Management says “Huh huh huh, you’re holding up product development” “you did the test wrong”.
You say “but we did it to the ASTM standard!”
Management says “take those results out, they were done wrongly.”
Then the packaging engineer (look at my username) says “Ok, then you sign the paperwork, I’m not.”
Management signs the paperwork.
Voila! Product met acceptance criteria!!