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Standard Operating Procedures for CLIA Compliance: Part 1

As a laboratory partner and compliance-centric organization, Ovation helps startup labs or labs new to the molecular space understand CLIA compliance. Each lab workflow and standard operating procedure in your lab must be documented to meet CLIA regulations.

By Matt Fleming

As a laboratory partner and compliance-centric organization, Ovation helps startup labs or labs new to the molecular space understand CLIA compliance. Each lab workflow and standard operating procedure in your lab must be documented to meet CLIA regulations.  That’s why we created a full eBook to help labs like yours build SOP templates and lab manuals that are based on decades of CLIA experience. In part one of this 3-part series, you’ll get an introduction into what CLIA is, who it impacts, and how to navigate the process of CLIA accreditation. Let’s dive in.

DISCLAIMER: These recommendations and template standard operating procedures are intended to be used for general purposes only. You should not rely upon the information in this eBook as a basis for making business, legal, or any other decisions. While we endeavor to provide the most accurate and updated information, Ovation.io makes no representations or warranties of any kind, express or implied about the completeness, accuracy, reliability, suitability, or availability with respect to this eBook for any purpose. This is not an all-encompassing guide to CLIA compliance. Any reliance you place on such material is therefore strictly at your own risk. 

What should a molecular diagnostics laboratory SOP include to be CLIA- compliant?

Every lab needs to understand CLIA compliance. And this is especially true for startup labs as they look to grow into the diagnostic industry. Tenured former Laboratory Director and Ovation laboratory expert, Pauline Ghee, has compiled an extensive outline of exactly what you’ll need to get your lab on the road to CLIA certification and laboratory best practices. Achieving CLIA accreditation ensures quality testing standards and expands the complexity of testing your lab can process. Your commitment to these standards accelerates the creation of new therapies for infectious diseases and rare genetic disorders. Ovation is proud to partner with labs like yours to make more specific treatments accessible for patients in need. 

Which labs need CLIA certification?

Before the Clinical Laboratory Improvement Amendments of 1988 or CLIA, testing was limited to independent hospitals and laboratories. Additionally, the complexity of tests and laboratories in which tests were performed was not considered. Now, CLIA has improved the standardization of laboratory testing and determined which laboratories have the capacity and ability to process certain test types. 

According to the CDC, The only laboratories NOT subject to CLIA standards are those that fall under the “waived tests” category. This CLIA-determined category includes simple tests with minimal chance of error or risk. These laboratories are exempt so long as they continue to perform testing in strict compliance with manufacturers’ instructions and regulations.*

Based on documented CLIA regulations, if your laboratory performs even one applicable test on “materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of the health of, human beings”, you are subject to CLIA regulation and should aim for accreditation.

How do I create a lab manual or lab standard operating procedure (SOP) to fulfill CLIA compliance?

Before diving into the steps to creating CLIA-compliant lab manuals or SOPs, you need to consider a few things.

  • Understand which type of CLIA certification your lab will need.
    • Certificate of Waiver: issued to a laboratory to perform only waived test.
    • Certificate for Provider-Performed Microscopy Procedures (PPMP): issued to a laboratory in which a physician, mid-level practitioner, or dentist performs no tests other than the microscopy procedures. Additionally, this certificate permits the laboratory to also perform waived tests.
    • Certificate of Registration: issued to a laboratory that enables the entity to conduct moderate or high complexity laboratory testing or both until the entity is determined by a survey to be in compliance with the CLIA regulations.
    • Certificate of Compliance: issued to a laboratory after an inspection that finds the laboratory to be in compliance with all applicable CLIA requirements.
    • Certificate of Accreditation: issued to a laboratory on the basis of the laboratory’s accreditation by an accreditation organization approved by CMS.
  • Ensure you are up-to-date on local and state regulations as they may include additional steps.
  • Ensure that all personnel are qualified by CLIA regulations for the duties they will perform on the outlined SOPNow that you’ve determined your specific certification type and laboratory staff requirements, you’re ready to start building your lab SOPs.

What are the foundational policies and procedures for CLIA compliance?

Begin your SOP documentation by understanding the standards for every person that will interact with a sample. These team members are responsible for upholding CLIA standards, and as such, must have the proper credentials and certifications required to maintain a high level of quality and accuracy in testing.

Compliant with the General Laboratory Systems 42 CFR § 493.1230 and other associated sections. 

    • ERGONOMIC POLICY: Personnel must have ergonomic work conditions, adjustable height of lab stools, minimization of repetitive motions required, etc.
      • PERSONNEL DOCUMENTATION
        • Copies of credentials of testing personnel from Accessioning to QC and release of results to patients include
          • Copy of certifications (Board or otherwise), Degrees, Diplomas, and other professional certifications by ASCP
          • Copy of transcripts that verify the credentials listed in 1.b.1.i
          • Awards and other achievements
          • Job descriptions that succinctly outline authorizations, immediate reporting supervisor and subordinates, and responsibilities
          • Documentation of all Training listed in below

How do you properly train personnel for CLIA compliance?

Based on the complexity of your lab’s sample testing your personnel will need specific training on the operational workflows. To start, your staff should have a lab SOP that meets each of the following standards. 

  • Training of personnel SOPs
    • Training records for testing protocols
    • Competency Assessments on the exact protocols used for testing patient specimens
    • Safety training for handling infectious agents in accordance with CDC protocols
    • Safety training to meet OSHA requirements including how to handle spills, etc.
    • Training of HIPAA and IT security
    • On-boarding and training on the LIMS platform

This is only the beginning of the steps you need to take to prepare for CLIA-compliant workflows. To read the remaining SOPs and documents your lab needs to achieve CLIA compliance, you can download the full “Standard Operating Procedures for CLIA Compliance” eBook here.

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