Serosep are thrilled to announce our RespiBio® Panel 1 (SARS-CoV-2) Test Kits have just received formal Validation under the Coronavirus Test Device Approvals (CTDA) legislation from the UK Health Security Agency.
For further information, check out the UK’s Register of Approved Products (under regulation 38A (5) of the Medical Devices Regulations 2002: COVID-19 test validation) at https://bit.ly/3zDu0df or go to https://bit.ly/3Blp4uB for further information on all respiratory panels in the RespiBio® range.
