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Therma Bright Inc V.THRM

Alternate Symbol(s):  TBRIF

Therma Bright Inc. is a Canada-based company, which is a developer and partner in a range of diagnostic and medical device technologies. It focuses on providing consumers and medical professionals with solutions that address medical and healthcare challenges. It is involved in developing, acquiring, manufacturing, and marketing proprietary healthcare and medical devices for the consumer and institutional marketplace. Its product offerings include Covid-19 diagnostic test product line, such as AcuVid COVID-19 Rapid Antigen Saliva Test and AcuVid COVID-19 Rapid Antibody Test; Sores & Bite Inflammation Therapy product line, such as InterceptCS Cold Sore Prevention System and TherOZap, and Muscle Pain & Blood Circulation Health Therapy product line, such as Venowave, which is a circulation booster designed to improve circulation in the lower extremities. Its products include Benepod, Inretio, AI4LYF, Invixa and Instatin, and others.


TSXV:THRM - Post by User

Comment by Smokey1958on Apr 21, 2021 1:21pm
158 Views
Post# 33037904

RE:I am surprised...

RE:I am surprised...

I'm glad that we have a system in place to safely monitor all sorts of medical applications ....but I'll go a step further, boubouna, and say this is ridiculous. Once they had ethics approval this should have been rubber stamped under some emergency order. It's no wonder that second last tweet put HC approval at the bottom of the list.

Also consider that all 9 other rapid antigen tests currently under review have been in this state for months now. There have been NO new additions. If there is a premium on the number of individuals carrying out the reviews then why not deny the application of the almost 100 other covid testing devices that are 1. unlikely to get approval and 2. even if they do that PCR niche has long been been filled.

I say this only in my disappointment in the system. THRM has much more potential in Central and South America, Europe and Africa.


boubouna wrote: I am surprised that we have not heard anything on the HC front....it is not like it is 'approval' for use from HC...it is an approval to start the clinical trials....i was/am expecting this news this week...anyone else feel same?

 

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