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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 goldyhawkon Feb 09, 2021 9:20am
155 Views
Post# 32511098

from a M.Meile email in previous post

from a M.Meile email in previous postI am certain that MInowledgement letter in R expected their acka couple weeks, but for the past 3 weeks FDA has put the brakes on all tests to take time to assess the impact of the variants....................................................................................................................................................................................................................................................................................................................................................................................................................................................................................I am certain thatt MIR expected their acknowledgement letter in a couple weeks, but for the past 3 weeks FDA has put the brakes on all tests to take time to assess the impact of the variants...----
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Mr Meile is telling the truth as he sees it , i think 
If FDA  is finished  assessing the impact of the variants , the letter of acknowledgement will arrive in the two weeks stated above 
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