Laboratory Reporting Module (MLRM)
Reporting Antigen Point of Care (POC) Test Results
Entities performing SARS-CoV-2 POC tests, including PCR and antigen tests are required to report ALL test results. This includes, but is not limited to, the Quidel Sofia SARS Antigen FIA and BD Veritor System.
The CalREDIE Manual Lab Reporting Module (MLRM) can be used to meet these reporting requirements. CalREDIE is the statewide reportable condition reporting system. MLRM allows users to report results for each patient tested directly to the local health department where the patient resides.
Steps to Report via CalREDIE MLRM:
- Complete the CalREDIE
Manual Lab Reporting Account Request Form
Each person who will be reporting results must complete this form.
- Submit completed account form to email@example.com .
- CalREDIE Helpdesk will process the account and send the user his/her login credentials.
- Review the CalREDIE
Manual Lab Reporting Quick Start Guide
This Guide walks the user through how to log in and submit a result in the MLRM.
- Login to the CalREDIE MLRM and begin submitting results.
- Contact firstname.lastname@example.org with any questions.
Controlling the spread of COVID-19 is a partnership and your timely reporting is essential toward ensuring a prompt public health response. We encourage you to enroll in the CalREDIE Manual Lab Reporting now to avoid any delays.
Please contact the Disease Control Program for any reporting questions at (805) 681-5280 or FAX at (805) 681-4069.