Working Together: Collecting Race, Ethnicity, and Language (REL) Data

As part of our efforts to meet the National Committee for Quality Assurance (NCQA) requirements, we started collecting race, ethnicity, and language (REL) data from our members on December 20, 2024. Health plans, including Premera, are required to collect this information to comply with NCQA standards and advance health equity. To fulfill this, we’re asking our members for their REL information through their secure member accounts and in the Premera mobile app. Participation in the REL questionnaire is 100% voluntary.

By analyzing this de-identified data, we can pinpoint gaps in care and design more equitable benefits and programs that better address the needs of diverse populations. This can help bridge the gap between need and care and improve access across our communities. Your role as a provider is critical in ensuring members receive the care and support they need.

Thank you for your continued partnership in advancing a more equitable approach to healthcare.