COVID-19 Testing Guide: Frequently Asked Questions



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Since the start of the COVID-19 pandemic, many clinical laboratories have quickly adopted SARS-CoV-2 testing to help meet high testing demands in the United States. With recent surges in the infection rate, test availability and turnaround time remain insufficient, with no definitive vaccine or curative drug solution in sight. Testing and quarantining remain the only proven methods to limit the spread of the virus and reduce its death rate.

If you are looking to implement COVID-19 testing in your lab or clinic, you need to know what pitfalls to watch out for and how to overcome the challenges associated with this task. These challenges include choosing the appropriate test to adopt, regulatory requirements, lack of clinical samples for validation testing, lack of reagents and test instruments, reagent incompatibilities and becoming a supplier of tests on a rapidly changing competitive market.

In this COVID-19 quick test guide from Zymo research, you will find all this and more. Sign up below to find the answers to these frequently asked questions:

    • What are the requirements for my lab to offer COVID-19 testing?
    • Should my lab offer testing as a lab-developed test or as an FDA-cleared test under Emergency Use Clearance?
    • What type of test should my laboratory offer? Serology, antigen or RT-PCR?
    • What factors should I take into account in choosing the right SARS-CoV-2 test?
    • Is it as easy as choosing the test I like the most and then delivering it to my lab?
    • How to reach the right audience for SARS-CoV-2 testing?

Sign up below to read now.


If you want more resources on this topic, check out the rest of our COVID-19 diagnostics in brief here!

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