Federal Register Recent Federal Regulation Documents - Justia Regulation Tracker - Justia Regulations Trackerhttps://regulations.justia.com/regulations/fedreg/agencies/department-of-health-and-human-services/2017/12/08?limit=200®isters=between&mode=atom2024-04-19T15:11:26-07:00Justia Inchttps://www.justia.com/Justia Regulations Trackerhttps://regulations.justia.com/images/justiafedregulations.gifCopyright 2011 Justia Inchttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26540.htmlNotice - Prospective Grant of Exclusive Patent License: N-Acetyl Mannosamine as a Therapeutic Agent2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26540Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26540.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26524.htmlNotice - Agency Information Collection Activities: Submission for OMB Review; Comment Request2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26524Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26524.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26495.htmlNotice - Submission for OMB Review; 30-Day Comment Request; A Generic Submission for Formative Research, Pre-testing, Stakeholder Measures and Advocate Forms at NCI (National Cancer Institute)2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26495Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26495.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26483.htmlProposed Rule - CLASS Condition of the Head Start Designation Renewal System2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26483Proposed Rulehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26483.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26472.htmlNotice - Agency Recordkeeping/Reporting Requirements Under Emergency Review by the Office of Management and Budget (OMB); Comment Request2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26472Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26472.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26470.htmlNotice - Report on the Performance of Drug and Biologics Firms in Conducting Postmarketing Requirements and Commitments; Availability2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26470Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26470.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26469.htmlNotice - Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments; Guidance for Industry; Availability2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26469Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26469.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26457.htmlNotice - Fostering Digital Health Innovation: Developing the Software Precertification Program; Public Workshop; Request for Comments2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26457Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26457.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26453.htmlNotice - Request for Information on the Office of Disease Prevention Strategic Plan for Fiscal Years (FY) 2019-20232017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26453Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26453.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26442.htmlNotice - Changes to Existing Medical Software Policies Resulting From Section 3060 of the 21st Century Cures Act; Draft Guidance for Industry and Food and Drug Administration Staff; Availability2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26442Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26442.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26441.htmlNotice - Software as a Medical Device: Clinical Evaluation; International Medical Device Regulators Forum; Guidance for Industry and Food and Drug Administration Staff; Availability2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26441Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26441.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26440.htmlNotice - Oncology Center of Excellence Listening Session; Public Meeting; Request for Comments2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26440Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26440.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26439.htmlNotice - Clinical and Patient Decision Support Software; Draft Guidance for Industry and Food and Drug Administration Staff; Availability2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26439Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26439.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26437.htmlNotice - Prescription Drug User Fee Act VI Commitment To Assess Current Practices of the Food and Drug Administration and Sponsors in Communicating During Investigational New Drug Development; Establishment of a Public Docket; Request for Comments2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26437Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26437.pdfhttps://regulations.justia.com/regulations/fedreg/2017/12/08/2017-26436.htmlNotice - Abbreviated New Drug Applications for Certain Highly Purified Synthetic Peptide Drug Products That Refer to Listed Drugs of Recombinant Deoxyribonucleic Acid Origin; Draft Guidance for Industry; Availability; Extension of Comment Period2017-12-08T00:00:00-08:002017-12-08T00:00:00-08:002017-26436Noticehttps://www.gpo.gov/fdsys/pkg/FR-2017-12-08/pdf/2017-26436.pdf