||SACHRP provides expert advice and recommendations to the Secretary, through the Assistant Secretary for Health, on issues and topics pertaining to or associated with the protection of human research subjects. The committee is composed of 11 appointed voting members, with additional ex-officio members from Common Rule government agencies. SACHRP presently has two working subcommittees, the Subpart A Subcommittee (SAS) and the Subcommittee on Harmonization (SOH). The March 13, 2018 meeting will include the following topics: an overview of secondary use of biospecimens and data; FAQs on the use of biospecimens, repositories and informed consent under the new and revised Common Rule; FAQs on the use of broad consent; recommendations regarding exceptions to the use of a single IRB; and the impact of the European Union’s General Data Protection Regulation on HHS human subjects research. Time is allotted for public comment.