RE: are we talking a billion or close to a billion25 Apr 2020 15:00
The WHO approval is for emergency use listing. It means that the tests can now be supplied by the United Nations and other procurement agencies supporting the COVID-19 response. The different tests suit different labs. For example 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.
With respect to Thermo Fisher they 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. So in short they have already the requisite approvals and do not emergency use listing