See the links below for more information on various aspects of the DMS Policy. If you have questions and don't see an answer below, feel free to reach out to a librarian.
This page provides a set of principles and best practices for creating a robust framework for protecting the privacy of research participants when sharing data under the NIH Policy for Data Management and Sharing (DMS).
Get resources and template language on obtaining informed consent for secondary research with data and biospecimens and for genomic research activities.
Understand some relevant considerations and best practices for developing partnerships with American Indian/Alaska Natives through the development and implementation of research studies.
