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If an NPI number is not available, please enter all zeros (0000000000). When adding a new testing location/facility under your organization, you will need the CLIA number associated with the facility, as well as the NPI number for the ordering provider at the facility or for your organization.After the organization account has been established, the administrator will be able to invite additional users to be administrators for the account or as standard users.If you have multiple testing facilities or locations within your organizations, coordinate among the different facilities to identify an administrator to create the account for your organization.As a new organization using SimpleReport, select “My organization is new to SimpleReport” when signing up.If you are interested in using SimpleReport for your testing program, you can sign up online.Digital Service which makes it easy for you and your testing staff to capture and send point-of-care test results directly to CDPHE.

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SimpleReport is a fast and free tool developed by CDC and the U.S.SimpleReport: Point-of-care rapid test reporting tool for testing providers. To onboard or for more information, email Read our FAQ document on case reporting for facilities that use electronic lab reporting.Option 1: Electronic laboratory reporting (ELR) Test result (positive, negative or inconclusive including quantitative ranges, if applicable).Test name/type (PCR, IgM, antigen, etc.).Testing lab name (name of testing lab, if applicable, or name of facility if doing point-of-care rapid testing).Ordering health care provider’s name, clinic address, and clinic phone number.Additional information on how to determine residency for case reporting.*If a patient is a student at a university, they should provide their local address at time of testing to ensure the local public health agency where their school is located is properly notified of the result.

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Patient’s home address* (address, city, state, ZIP code).Name of disease or condition (i.e., COVID-19).Required components for reporting based on Colorado Board of Health Rules and Regulations Self-administered home tests are not required to be reported.

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All positive antigen and positive, negative, and inconclusive molecular test results for SARS-CoV-2 testing conducted as part of a clinical trial must be reported electronically by the testing laboratory.Facilities that are designated as sentinel surveillance sites should continue to submit surveillance samples according to sampling plans.If a laboratory is performing SARS-CoV-2 testing that generates a sequence or lineage result, this information is required to be reported to CDPHE by Board of Health Rules and Regulations and submission of clinical material may be requested.All positive, negative, and inconclusive, nucleic amplification/molecular (e.g., RT-PCR) SARS-CoV-2 test results must be reported electronically by laboratories.COVID-19 results are required to be reported in four (4) working days. Providers must also report all positive, negative, and inconclusive COVID-19 test results for non-point-of-care NAAT tests (e.g., RT-PCR, those sent out to a lab for testing).All positive test results for rapid point-of-care COVID-19 tests must be reported to public health.Engage with the Water Quality Control Division.Toxicology and environmental epidemiology.Test & Fix Water for Kids at Family Child Care Homes.Colorado Legacy Land/Lincoln Park Superfund site.Hazardous materials and waste management.

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