Draft Guidance – When Continuing Review Is Not Required During the 6-Month Delay Period of July 19, 2018 through January 20, 2019
Links to the Draft Guidance and Federal Register Notice of Availability:
The draft guidance can be accessed at When Continuing Review is not Required During the 6-Month Delay Period of July 19, 2018 through January 20, 2019.
A copy of the Federal Register notice announcing the availability of the draft guidance for comment can be accessed in either HTML or PDF formats at the Government Printing Office's Federal Digital system (FDsys) website.
The draft document provides guidance on the HHS regulations for the protection of human research subjects at 45 CFR part 46 related to the circumstances in which continuing review of research is not required. In particular, this guidance applies to research that transitions to comply with the 2018 Requirements during the 6-month delay period from July 19, 2018 through January 20, 2019. This guidance only applies during the 6-month delay period. It is intended for Institutional Review Boards (IRBs), investigators, HHS funding agencies, and others that may be responsible for the review, conduct, or oversight of human subjects research conducted or supported by HHS.
How to Access Comments that Have Been Submitted:
With your Web browser, go to the Federal eRulemaking Portal: http://www.regulations.gov. Enter the docket ID number HHS-OPHS-2018-0013 in the "Enter Keyword or ID" field and click on "Search." On the next web page, the next web page, click "Open Docket Folder", on next page, click "View all documents and comments in this Docket". The list of comments extends over more than on page, and additional comments can be accessed by clicking the forward or back buttons at the bottom of the page. Note that some comments include attachments that can be opened.
When and How to Submit Comments:
Submit comments by 8/24/2018.
You may submit comments, identified by docket ID number HHS-OPHS-2018-0013, by one of the following methods:
- Federal eRulemaking Portal: http://www.regulations.gov. Enter the above docket ID number in the "Enter Keyword or ID" field and click on "Search." On the next web page, click on the "Submit a Comment" action and follow the instructions.
- Mail/Hand delivery/Courier [For paper, disk, or CD-ROM submissions]: Irene Stith-Coleman, Ph.D., OHRP, 1101 Wootton Parkway, Suite 200, Rockville, MD 20852.
OHRP strongly encourages commenters to submit comments via the Federal eRulmaking Portal. Comments received, including any personal information, will be posted without change to the docket at http://www.regulations.gov as they are submitted, usually within 1 week after submission. While the comment period remains open, individuals may also provide comments in response to already submitted comments that have been posted to the docket.
For Further Information Contact:
Irene Stith-Coleman, Ph.D., OHRP, 1101 Wootton Parkway, Suite 200, Rockville, MD 20852, 240-453-6900; e-mail Irene Stith-Coleman@hhs.gov.
Content last reviewed on July 25, 2018