Federal Register Recent Federal Regulation Documents - Justia Regulation Tracker - Justia Regulations Trackerhttps://regulations.justia.com/regulations/fedreg/agencies/department-of-health-and-human-services/2013/12/04?limit=200®isters=between&mode=atom2024-11-24T16:34:55-08:00Justia Inchttps://www.justia.com/Justia Regulations Trackerhttps://regulations.justia.com/images/justiafedregulations.gifCopyright 2011 Justia Inchttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-29020.htmlNotice - National Institute of General Medical Sciences; Notice of Closed Meeting2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-29020Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-29020.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-29010.htmlNotice - Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medical Devices; Third-Party Review Under the Food and Drug Administration Modernization Act2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-29010Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-29010.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-29008.htmlNotice - Center For Scientific Review; Notice of Closed Meetings2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-29008Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-29008.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28991.htmlNotice - Agency Information Collection Activities; Submission to OMB for Review and Approval; Public Comment Request2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28991Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28991.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28990.htmlNotice - Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Biological Products: Reporting of Biological Product Deviations and Human Cells, Tissues, and Cellular and Tissue-Based Product Deviations in Manufacturing; Forms FDA 3486 and 3486A2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28990Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28990.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28989.htmlNotice - Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Human Tissue Intended for Transplantation2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28989Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28989.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28980.htmlProposed Rule - Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act; Request for Nominations2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28980Proposed Rulehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28980.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28979.htmlProposed Rule - List of Bulk Drug Substances That May Be Used in Pharmacy Compounding; Bulk Drug Substances That May Be Used To Compound Drug Products in Accordance With Section 503A of the Federal Food, Drug, and Cosmetic Act2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28979Proposed Rulehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28979.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28978.htmlProposed Rule - Bulk Drug Substances That May Be Used To Compound Drug Products in Accordance With Section 503B of the Federal Food, Drug, and Cosmetic Act, Concerning Outsourcing Facilities; Request for Nominations2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28978Proposed Rulehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28978.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28963.htmlNotice - Draft Guidance; Pharmacy Compounding of Human Drug Products Under Section 503A of the Federal Food, Drug, and Cosmetic Act; Withdrawal of Guidances2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28963Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28963.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28962.htmlNotice - Draft Guidance for Industry on Registration for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act; Availability2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28962Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28962.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28961.htmlNotice - Guidance for Industry and Food and Drug Administration Staff; Civil Money Penalties for Tobacco Retailers: Responses to Frequently Asked Questions; Availability2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28961Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28961.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28960.htmlNotice - Draft Guidance for Industry on Interim Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act; Availability2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28960Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28960.pdfhttps://regulations.justia.com/regulations/fedreg/2013/12/04/2013-28887.htmlNotice - Findings of Research Misconduct2013-12-04T00:00:00-08:002013-12-04T00:00:00-08:002013-28887Noticehttp://www.gpo.gov/fdsys/pkg/FR-2013-12-04/pdf/2013-28887.pdf