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Sona Nanotech Inc C.SONA

Alternate Symbol(s):  SNANF

Sona Nanotech Inc. is a nanotechnology life sciences company that has developed multiple methods for the manufacturing of various types of gold nanoparticles. The Company is engaged in the research and development of its technology for use in multiplex diagnostic testing platforms and biomedical applications. Its gold nanotechnologies are adapted for use in applications, as a safe and delivery system for multiple medical treatments, for the approval of various regulatory boards, including Health Canada and the Food and Drug administration (FDA). Its gold nanorod particles are manufactured without the use of CTAB (cetyltrimethylammonium), eliminating the toxicity risks associated with the use of other gold nanorod technologies in medical applications. The Company leverages its core proprietary gold nanorod (GNR) manufacturing technology and laboratory assets to focus on the development of diagnostic tests and biologic reagents, and the advancement of its GNR intellectual property.


CSE:SONA - Post by User

Post by Awsm11on Jul 15, 2020 10:18am
204 Views
Post# 31270158

Interested Partners ... come on down...SONA is taking orders

Interested Partners ... come on down...SONA is taking ordersDear Interested Partners,
 
Sona Nanotech Inc. is pleased to announce that its rapid detection, COVID-19 antigen test validation studies of performance levels have resulted in a test sensitivity of 96%, test specificity of 96% and a Limit of Detection ("LOD") of 2.1 x 102 TCID50. Validation studies were conducted to assess the test's potential clinical performance using 30 nasopharyngeal samples from healthy individuals who were presumed negative for COVID-19.
 
For additional details, please read July 2nd Press Release: https://sonanano.com/sona-nanotech-announces-validation-results-for-its-covid-19-antigen-test/
 
As the pandemic continues and the understanding of COVID-19 improves, regulators have placed greater emphasis on clinical, 'in-field' evaluations of rapid tests at the point of care to ensure they can be deployed with confidence. Following consultation with MRIGlobal and the FDA, Sona will enter into independent clinical, in-field evaluation studies to generate the data to support its analytical and clinical data as part of the submission it will make to Health Canada and the FDA for emergency use authorization ("EUA") approval.
 
The Company is inviting interested partners, the opportunity to begin partnership agreement discussions. Please advise on your interest in proceeding, and we would look forward to speaking with you at your earliest convenience.
 
 
 
Many Thanks,
Dianna
 
Dianna Lesperance  | Business Development Analyst
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