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Re: vator post# 710682

Sunday, 08/04/2024 8:57:48 AM

Sunday, August 04, 2024 8:57:48 AM

Post# of 723460
Why are you arguing my point that it is the Regulator's responsibility to never accept any submitted trial results at face value, irrespective of an external party sign off prior to submission?

Would you buy a car, on the sole basis that the salesman said that it had no defects ?

NWBO is not exempt from the normal Regulatory due diligence processes , which are even more stringent, post covid.

So you all need to get your heads out of your arses, and accept that this rubber-stamping 'special relationship' between NWBO & MHRA is now over.

This Biotech firm now longer wags the Regulator's tail, as NHS England has now grab the lead.

As I said previously, I am unashamedly on the side of vulnerable patients & my Health service, to protect both from commercially incentivised financial exploitation.

If you don't like that, I DO NOT CARE
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