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The FDA has issued Emergency Use Authorizations (EUA) for numerous molecular and antigen tests for detection of SARS-CoV-2 (COVID-19). Our Viral Transport Media is listed per FDA guidance, “Enforcement Policy for Viral Transport Media during the Coronavirus 2019 (COVID-19) Public Health Emergency.”  The VTM is manufactured in the LaunchWorks CDMO facility which is FDA registered, cGMP compliant, and ISO 13485:2016 certified.

VTM Specimen Kit:

 - 1 tube with 3 mLs of sterile LaunchWorks VTM
 - Biohazard bag - tube labeled per CDC instructions
 - Absorbent pad

Options:

 - Nylon-flocked NP swab
 - Barcode or QP-coded
labels (up to 3)
 - Patient Card
 - UN 3373 Return Box

Swab Specifications:

 - Naseopharyngeal swab
 - Individually packaged
 - Nylon flocked
 - 155mm, 80 mm breakpoint

 - FDA-registered Manufacturer
 - Ethylene Oxide Sterlization
 - 2 year shelf-life
 - CE-marked

Launchworks VTM Recipe:

 - Fetal Bovine Serum (sterile, heat
inactivated, USDA approved)
 - Hanks Balanced Salt Solution
(no phenol red)