Federal Register Recent Federal Regulation Documents - Justia Regulation Tracker - Justia Regulations Trackerhttps://regulations.justia.com/regulations/fedreg/agencies/department-of-health-and-human-services/2007/10/15?limit=200®isters=between&mode=atom2024-11-23T14:35:44-08:00Justia Inchttps://www.justia.com/Justia Regulations Trackerhttps://regulations.justia.com/images/justiafedregulations.gifCopyright 2011 Justia Inchttps://regulations.justia.com/regulations/fedreg/2007/10/15/E7-20304.htmlNotice - Pediatric Advisory Committee; Notice of Meeting2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:00E7-20304Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/E7-20304.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/E7-20302.htmlNotice - Pediatric Advisory Committee; Notice of Meeting2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:00E7-20302Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/E7-20302.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/E7-20291.htmlNotice - Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Focus Groups as Used by the Food and Drug Administration2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:00E7-20291Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/E7-20291.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/E7-20282.htmlNotice - Draft Guidance for Industry on Antibacterial Drug Products: Use of Noninferiority Studies to Support Approval; Availability2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:00E7-20282Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/E7-20282.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/07-5074.htmlNotice - Draft Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:0007-5074Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/07-5074.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/07-5073.htmlNotice - Draft Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application; Availability2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:0007-5073Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/07-5073.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/07-5060.htmlNotice - Statement of Organization, Functions, and Delegations of Authority2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:0007-5060Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/07-5060.pdfhttps://regulations.justia.com/regulations/fedreg/2007/10/15/07-5057.htmlNotice - Meeting of the National Advisory Council for Healthcare Research and Quality2007-10-15T00:00:00-07:002007-10-15T00:00:00-07:0007-5057Noticehttp://www.gpo.gov/fdsys/pkg/FR-2007-10-15/pdf/07-5057.pdf