Relevant post from AVCT5 Aug 2021 19:42
All the below is copied from a post on a board that I can not name but I will name because it is a copied post. AVACTA! The poster is a prolific nearly 8k posts poster - PL75!
It is very relevant for here as well. Bighero will give credit where credit is due and he has smallhero status for a day.
“I've previous despaired that my local Labour MP didn't respond to the email I sent inquiring about the new legislation and the free pass being given to Innova and others. The email I sent was the template we had on here (many thanks), with the addition of raising the same concerns for Healgen and highlighting AffiDx performance in identifying the infectious as a green light test.
Some credit is finally due. Today I received a written copy of a letter that she has sent to Sajid Javid where she reiterated the main points from the email/attached links (including the FDA throw them in the trash quote) and has asked him for an urgent response to these Qs:
- Confirm that testing on the Innova tests carried out in accordance with the DHSCs Instructions For Use have taken place?
- Confirm the revised sensitivity rating achieved by the Innova tests when the tests were carried out in accordance with revised DHSC IFU?
- If this testing has not been carried out, please can you confirm what plans you have in place to carry out this testing and when it is due to take place?
She closes her letter by asking:
- Please can you confirm why the government is continuing to invest in Innova Tests for community testing, when there is an opportunity to support British business whilst also providing the community with better quality tests that have been specifically designed for this type of testing?
Obviously, no doubt the govt will spew out the usual dismissive bile, but every little helps.
She's has also forwarded on my email to Sajid and asked me if I have any thoughts on any parliamentary questions that should be raised. Fire away with your ideas - the more the merrier and I'll draft them up and get them sent across....
She noted that whilst the legislation was approved, red flags were raised by the Regulatory Committee and that revisions are due.”