clia inspection checklist 2021

Drug Approvals and Databases, Recalls, Market Withdrawals and Safety Alerts, Resources for Information | Approved Drugs, Clinical Investigator Inspection List (CLIIL), Clinical Investigator Inspection List (Search), Clinical Investigator Inspection List Zip File, Clinical Investigator Inspection List (CLIL) Database Codes, Clinical Investigations Compliance & Enforcement, To protect the rights, safety, and welfare of human research subjects, To verify the accuracy, reliability, and integrity of clinical and nonclinical trial data submitted to FDA. If you do not allow these cookies we will not know when you have visited our site, and will not be able to monitor its performance. If you identify any errors with your logs, it's important to develop and document your own corrective plan of action. The customized checklist version created for on-site inspections and self-evaluations may not list all of these requirements. UPDATED. Be advised that information contained herein is intended to serve as a useful reference for informational purposes only and is not complete clinical information. Accreditation Checklists Developed with input from more than 500 pathologists and laboratory experts, our 21 discipline-specific accreditation checklists provide a clear roadmap for not only achieving accreditation but also for running a high-quality laboratory. Therefore, laboratories should always take steps to maintain accurate and consistent quality control (QC) records. Clinical Laboratory Improvement Advisory Committee (CLIAC), Centers for Disease Control and Prevention. These must include procedures for all phases of testing performed by the laboratory; define quality control by the frequency, type and number used; include corrective action protocols; list critical values when appropriate, with follow up actions; and specimen acceptability requirements. Image source: /content/dam/soi/en/web/idph/files/images/clia-photo1.jpg. number. "Sometimes it's worth it to invest in working with experts who can bring peace of mind throughout the process," says Bakken. lock %%EOF /CreationDate (D:20200514090514-05'00') Laboratories perform their own mock inspections, but some facilities and physician offices may opt to contract this out, either for a stand-alone mock inspection or for ongoing support. 664 0 obj <> endobj While laboratories issued a certificate of waiver or certificate for provider performed microscopy are not subject to biennial inspections, CMS or its representatives may conduct inspections at any time during the laboratory's hours of operation to: Waived and PPM laboratories must comply with all of the basic inspection requirements. to Default, California Conference of Local Health Officers, Communicable Disease Control And Prevention, Chronic Disease Injury Prevention Agenda 1-5-2017, Chronic Disease Injury Prevention Agenda 2-15-2017, Chronic Disease Injury Prevention Agenda 3-2-2017, Center for Chronic 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You can verify receipt of your forms by calling 503-693-4125 or by e-mailing LC.info@odhsoha.oregon.gov. The CLIA historical numbers file is from January 2022. All information is provided in good faith, however, we make no representation or warranty of any kind regarding its accuracy, validity, reliability, or completeness. Quality, Safety & Oversight - Certification & Compliance, How to Apply for a CLIA Certificate, Including International Laboratories, Accreditation Organizations/Exempt States, Certification Boards for Laboratory Directors of High Complexity Testing, CLIA Regulations and Federal Register Documents, CLIA Related Hearing Decisions and Compliance Topics, Individualized Quality Control Plan (IQCP), State Agency & CLIA Operations Branch Contacts, CME Courses for Laboratory Directors of Moderate Complexity Laboratories, /Regulations-and-Guidance/Legislation/CLIA/Downloads/CLIASA.pdf (PDF), https://public.govdelivery.com/accounts/USCMS/subscriber/new?topic_id=USCMS_12461, CLIA of 1988 Proficiency Testing Regulations Related to Analytes and Acceptable Performance (CMS-3355-F) FAQ Sheet 7/7/2022 (PDF), CLIA University Lab Testing 8/28/2020 (PDF), Frequently Asked Questions (FAQs), Abbott i-STAT - Updated 12-08-2022 (PDF), Research Testing and CLIA 12/10/2014 (PDF), Partners in Laboratory Oversight 09/2006 (PDF), Live Blood Cell Analysis Under CLIA 03/17/2017 (PDF), MLN006270 - CLIA Program & Medicare Lab Services December 2021 (PDF), CLIA Fee, Histocompatibility, Personnel, Alternative Sanction NPRM CMS-3326-P 07/22/2022 (PDF), CLIA SARS-CoV-2 Point Of Care Test Enforcement Discretion - Updated 10/7/2022 (PDF), SARS-CoV-2 Point of Care Testing and CLIA Certificate of Waiver Applications - Updated 12-17-2020, Frequently Asked Questions FAQs CLIA Guidance During the COVID-19 Emergency - Updated 12-17-2020, How Laboratorians Can Safely Calculate Workload for FDA-Approved Semi-Automated Gynecologic Cytology Screening Devices 08/05/2015, CDC PPMP - A Focus on Quality Practices Booklet, All other questions about the CLIA program should be submitted to.