RE: Yourgene18 Apr 2020 19:12
The WHO approved Roche and Novacyt for emergency use listing. It meant that the tests can now be supplied by the United Nations and other procurement agencies supporting the COVID-19 response. The genesig Real-Time PCR Coronavirus (COVID-19) (Primerdesign, United Kingdom) is an open system more suitable for laboratories with moderate sample testing capacity, while the cobas® SARS-CoV-2 for use on the cobas® 6800/8800 Systems (Roche, United States of America) is a closed system assay for larger laboratories. That is I believe the key difference.
Separate to receiving FDA approval, Thermo Fisher received the CE mark in the European Union for its diagnostic test to detect nucleic acid from SARS-CoV-2, the virus that causes COVID-19 on the on 26th March 2020. In addition to receiving the designated approvals in the U.S. and E.U., Thermo Fisher's diagnostic test has received the designated approvals in Canada, Singapore, India, Australia and New Zealand.
I would agree with the statements that regardless of any worries to impairment to trading figures that, subject to testing capacity, Yourgene have quite a few opportunities with their positioning with Thermo Fisher and Novacyt. Also within the NIPT sphere with Illumina.