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This is a read only version of the page. CDC Newborn Screening Quality Assurance ProgramToggle navigation Biochemical PT PT Information Biochemical Analyte Selection Biochemical Specimen Data Entry Biochemical Review/Submit Data ALD Entry ALD Review/Submit CAH Entry CAH Review/Submit Hb Entry Hb Review/Submit HIV Entry HIV Review/Submit LSD Entry LSD Review/Submit TOXO Entry TOXO Review/Submit Molecular PT CFDNA Entry CFDNA Review/Submit SMA Entry SMA Review/Submit TREC Entry TREC Review/Submit QC Educational Programs Hb Educational Data Entry Hb Educational Review/Submit Page Help Help FAQS Add/Remove Users NSQAP Portal User Guides PT Portal Entry Instructions PT Assay and Reporting Instructions Sign in Please use Microsoft Edge or an updated browser to access the portal to ensure there are no browser compatibility issues, thank you. Newborn Screening Quality Assurance Program Previous Previous Next Welcome to the NSQAP Participant Portal Newborn Screening identifies conditions that can affect a child’s long-term health or survival. CDC’s Newborn Screening and Molecular Biology Branch manages the Newborn Screening Quality Assurance Program (NSQAP) to enhance and maintain the quality and accuracy of newborn screening results. The program provides training, consultation, guidelines, and dried blood spot proficiency testing and quality control materials to state public health laboratories and other laboratories responsible for newborn screening in the U.S. and many other countries. Learn more »A2LA Accredited PT Provider A2LA Accredited PT Provider CDC’s Newborn Screening and Molecular Biology Branch (NSMBB) has been granted ISO/IEC 17043 accrediation by the American Association for Laboratory Accreditation (A2LA). Please consult A2LA Certification #4190.01 for a list of accrediated NSMBB proficiency testing programs. -Request Participation (New Participants Only) If you are interested in participating in this program, complete the Participant Request Form. Products and shipping are free for participating laboratories. Laboratories are responsible for the cost of required documentation, import fees, taxes, and other costs. Participants must report data for each product requested .NSQAP Public Reports If you would like to access any previous quarterly and annually public reports, click here. Calendar: Key Dates and Events Click to view Calendar»Click to view Calendar» Feedback Please click here to submit any Feedback » Contact Us Please click here for additional questions » Get Help Browse the KB Create Case Contact usAbout NSQAP Self-Service Portal This program is cosponsored by the Centers for Disease Control and Prevention (CDC) and the Association of Public Health Laboratories (APHL). Copyright © 2024. All rights reserved. Information No Fear Act FOIA Accessibility Privacy Disclaimer Vulnerability Disclosure Policy Questions? Contact...