RE: Did you read that ?22 May 2024 17:11
@B2H
wrt training, there will have been a train the trainer approach from nova.
Nova will have trained usually senior staff in each lab. Once both nova and the lab were happy with using the equipment it would have been signed off as all OK.
It would then fall to those lab staff to cascade that training out to the rest of appropriate staff (be interesting to know in the labs that had high failure rates, what level of staff were using the Qs. Were they qualified biomedical scientists? Or unqualified APs associated practitioners)
Another question for twiggers to ask perhaps.
Normal training protocols in a lab requires teaching the technique, then observation of the trainee using machine, if OK person signed off for routine use.
This is standard practice, not 100% sure if its mandated but accreditation of labs, requires evidence of robust (lol) training protocols.
Was this model followed by all labs?
Can they provide evidence of robust training protocols of ALL staff using the Qs
Again, more questions for Twiggers to ask.
Were the correct decontamination procedures followed, all the time.
Can they provide the SOPs for the decontamination procedure, does that align with the IFU from Nova?
As I've said before, so many potential points of failure.
If the dhsc cannot provide this info (who knows tbf) in conjunction with 2 labs having no issues, it casts a not insignificant doubt on it being 100% a faulty test.
My personal opinion FWIW knowing the above facts, doing a root cause analysis of failure would be to immediately look to user error before even considering a faulty test.
I'm a scientist, not a lawyer so I don't know what the burden of proof required to decide is, in contract law.
But there is a lot in what I've written previously that would cast serious doubt of it being a faulty test.
Given the propensity of my posts to go missing in action, somebody of influence is reading these posts.
Please copy in case it goes missing again.
As you were
P.