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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

Post by wanttoretireearlyon Dec 19, 2021 4:47am
482 Views
Post# 34244361

FDA’s forced hand drops Pfizer’s Bombshell Safety Document

FDA’s forced hand drops Pfizer’s Bombshell Safety DocumentThe highly confidential Pfizer documents, which have been synonymous with the extreme lack of transparency revealed by the actions of pivotal governmental agencies, over the past 20 months, lead critics of the official narrative to demand show us the data, is finally being revealedwell sort of, the first few hundred redacted pages out of a trove of 451,000. The FOIA request was issued by a group of over 30 scientists and academics who filed a civil action lawsuit against the agency because they failed to fully comply with the request, since less than 1% of the documentation was released and with the FDA taking the position that all the data would be shared by 2076. Subsequently, the governmental agency had the audacity to push the date back even further to 2096. This was due to their recent disclosure of the existence of thousands of additional pages, totaling 451,000 versus the originally stated 320,000 pages. However, the rate at which the FDA is willing to release the documentation has not changed and remains at 500 pages a month. Its worth noting that it took the FDA only 108 days to review all of Pfizers documentation before authorizing the Pfizer BNT162B2 vaccine for emergency authorization use on December 1, 2020. more here: https://trialsitenews.com/fdas-forced-hand-drops-pfizers-bombshell-safety-document/
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