Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.

MedMira Inc V.MIR

Alternate Symbol(s):  MMIRF

MedMira Inc. is a Canada-based developer and manufacturer of Rapid Vertical Flow (RVF) diagnostics. The Company's tests provide hospitals, labs, clinics and individuals with instant disease diagnosis, such as human immunodeficiency virus (HIV), syphilis, hepatitis, and SARS-CoV-2, in three steps. The Company is engaged in the business of research, development and manufacturing of rapid diagnostics and technologies. Its research is focused on specific areas of the broader diagnostics market, namely the rapid, point-of-care, and in vitro sectors. Its tests are sold globally under the REVEAL, REVEALCOVID-19, Multiplo and Miriad brands. Based on its patented Rapid Vertical Flow Technology, the Company's rapid HIV test has regulatory approvals in Canada, the United States, China and the European Union. Its manufacturing facilities are located in Halifax, Nova Scotia, Canada. It provides access to its RVF Technology for researchers, developers, and biotech companies on a license basis.


TSXV:MIR - Post by User

Post by august202013on May 15, 2021 8:39pm
426 Views
Post# 33210644

USA FDA HAVE EVERY INTENTIONS TO ISSUE EUA AFTER JUNE

USA FDA HAVE EVERY INTENTIONS TO ISSUE EUA AFTER JUNECome June 2021 after 50 % to 60 % of all USA are FULLY VACCINATED and no more mandatory use of masks then USA FDA's EUA ( NOT FULL AUTHORISATION) will be issued for the COVID19 TEST KIT PLUS. Appears Handicapped but would still be manageable as then can try to work into the various AIRPORTS and PORTS of entry of Countries of world as there will be a need to TEST the individuals immunity. Question is 'why HAVE wait for God Father's (USA FDA's) blessing ? Or please enlighten US if that is another of USA FDA's RULE. Or have MIR not learned the LESSON that Pfizer was not required to withdraw their earlier authorization when they submitted another. MIR must TRY to penetrate into ALL COUNTRIES through the individual countries FDA NOW ! Or for ever PRICED at these LEVEL. Have to market the COVID19 TEST KIT PLUS when is still relevant as it MIGHT not be relevant when the whole world is fully vaccinated by then it is only good to be in the WHO museum.
<< Previous
Bullboard Posts
Next >>