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About NQRN

The National Quality Registry Network (NQRN®) is a voluntary network of organizations operating registries and others interested in increasing the usefulness of clinical registries to measure and improve patient health outcomes.

NQRN overview
NQRN coordinating task force recommendation 2011

Committees

The NQRN Steering Committee consists of 12 members, representing medical professionals, registry stewards, experts in registry technology, payers, and consumer/patient users. The Steering Committee provides strategic direction and oversight for NQRN activities.

The NQRN Council is composed of members, plus Federal Government liaisons, who represent registry stewards and participants, non delivery system registry users, and supporting technologies.

NQRN Council roster
NQRN Steering Committee roster
NQRN roles and responsibilities
NQRN conflict of interest policy

Resources

What is a Clinical Data Registry?
Clinical Registry FAQ
National Clinical Registry Inventory
Registry Vendor Assessment
Clinical Registry Maturational Framework
Clinical Registry Maturational Framework brief
Qualified Clinical Data Registry (QCDR) tip sheet

Contact us

You may contact us with any questions or comments at:

Seth Blumenthal
American Medical Association
330 N. Wabash Avenue, Suite 39300
Chicago, Ill. 60611

(312) 464-4049
seth.blumenthal@ama-assn.org

Additional Resources

NQRN Website Banner Program

The National Quality Registry Network (NQRN®) provides the opportunity to promote your participation in the NQRN by placing a clickable NQRN banner on your website.

If you wish to participate in this program, please contact us.

NQRN Collaboration Portal

Interact with fellow NQRN participants through topical discussion forums and access documents, a calendar of events, and other resources.

NQRN Council participation is required to use the Portal. If you are already participating in the Council and want to start using this new tool, please contact us.