RE:RE:RE:Read between the lines....NRV - my read of the NR, is that they have completed the 100 tests, which then they earlier reported that this is when the final design/ science would be 'locked in'. Now, people they are going to experiment on human live subjects, they need ethical approval. This approval shouldn't take long, as it is not evasive, nor are they using a concept of deception to determine results. They aren't using a live control group either; since the 300 persons will be those likely already identified as Covid positive. The AcuVid then will be used to see if it receives the same results.
This study of the 300 pers, is the required study for Health Canada approval.
When I read HC's website, they set the scope of what they require for submissions; which THRM is following. Once this study is completed, they can apply to HC for their approval.
HC may take 45 days to approve applications; maybe quicker due to Covid fast tracks.
The timeline is getting nearer. My best estimate would be potentially mid May to receive back HC approval (could be early or late May, but I'm going to stick with mid May).
During this time before now and then, they will be already lining up manufacturers as previously detailed in the other NRs. Now their design is "locked in" they are obviously happy with its performance and results. A manufacturer will be being sourced to design it to their specs.
Production could commence as soon as HC approval is given, should THRM get their ducks in a row as I am predicting. Thus far, they have proven competent in this regard.
Good luck everyone! The THRM Tsunami is coming!