NACC maintains a library of best practice resources to support consistent, high-quality research across the Alzheimer's Disease Research Center (ADRC) network. Developed through collaboration with NIA-convened working groups, these resources address key aspects of center operations, from biospecimen handling and participant engagement to data management and institutional governance.

These resources are intended as practical guidance for new centers and any centers launching a new research line. They should not be construed as requirements for center activities.

Because many of these areas continue to evolve, we periodically review and update these guidelines. If you have suggestions for new topics or notice content that may be outdated, please use the feedback link at the bottom of this page.

Participant Engagement and Clinical Operations

These resources support participant-facing workflows, including enrollment, consent, and return of results.

Biospecimen Acquisition, Processing, and Storage

These resources cover standardized collection, handling, and storage of biological specimens.

Neuropathology

These resources support postmortem tissue workflows and digital pathology infrastructure.

Data Management, Informatics, and Study Quality

These resources address data infrastructure, sharing practices, and standards for research rigor.

Outreach, Recruitment, and Community Engagement

These resources support community-based participation and engagement with state and federal stakeholders.

Center Administration and Governance

These resources address institutional operations, oversight, and planning.

* Included in the original working group guidance. A single PDF of the collected working group guidance is available for reference here.


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