Department: DEPARTMENT OF HEALTH AND HUMAN SERVICES
Years: 20002001200220032004200520062007200820092010201120122013[FR Doc E6-21138] 126. Industry Exchange Workshop on Food and Drug Administration Clinical Trial
The Food and Drug Administration (FDA) Los Angeles District, in cooperation with the Society of Clinical Research Associates (SoCRA), is announcing a workshop on FDA clinical trial statutory and regulatory requirements. This 2day workshop for the clinical research community targets sponsors, monitors, clinical investigators, institutional
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-21123] 127. Privacy Act of 1974; Report of New System of Records
In accordance with the requirements of the Privacy Act of 1974, CMS is proposing to establish a new system of records (SOR) titled ``Medicare Integrated Data Repository (IDR),'' System No. 0970 0571. In December 2003, Congress passed the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) (Pub. L. 108173), that amends Title
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Medicare & Medicaid Services
[FR Doc 06-9666] 128. Proposed Information Collection Activity: Comment Request
Proposed Projects
Title: Evaluation of the Mentoring Children of Prisoners (MCP) Program.
OMB No. New Collection.
Description: The Promoting Safe and Stable Families Amendments, as reauthorized (2006), amended Title IVB of the Social Security Act (42 U.S.C. 629629e) providing funding for nonprofit agencies that recruit, screen, train,
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Children and Families Administration
[FR Doc E6-21146] 129.
On November 1, 2006, the U.S. Department of Health and Human Services (HHS) issued a notice in the Federal Register (FR Doc. Vol 71, No. 211, pages 6428264284) to request input from the public and private sectors on plans for developing and using resources involving health information technology and genetic and molecular medicine, with specific
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Health and Human Services Department
[FR Doc E6-21133] 130. Supplements and Other Changes to Approved New Animal Drug Applications
The Food and Drug Administration (FDA) is amending its regulations on supplements and other changes to approved new animal drug applications (NADAs) or abbreviated new animal drug applications (ANADAs) to implement the manufacturing changes provision of the Food and Drug Administration Modernization Act of 1997 (the Modernization Act). The final
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc 06-9657] 131. Food Labeling: Nutrition Labeling of Dietary Supplements on a ``Per Day''
The Food and Drug Administration (FDA) is amending its nutrition labeling regulations for dietary supplements to provide that the quantitative amount and the percent of Daily Value of a dietary ingredient may be voluntarily presented on a ``per day'' basis in addition to the required ``per serving'' basis when a recommendation is made on the
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-21132] 132. Agency Information Collection Activities; Submission for Office of Management
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-21192] 133. Proposed Data Collections Submitted for Public Comment and Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, the Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a
Published: 2006-12-13 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention
[FR Doc E6-21040] 134.
The CERHR announces the availability of the draft expert panel report for bisphenol A on December 15, 2006, from the CERHR Web site (http://cerhr.niehs.nih.gov) or in printed text from CERHR (see FOR FURTHER INFORMATION
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc E6-21019] 135. Over-the-Counter Human Drugs; Labeling Requirements; Proposed Rule
The Food and Drug Administration (FDA) is proposing to amend its final rule that established standardized format and content requirements for the labeling of overthecounter (OTC) drug products (Drug Facts Rule, codified at 21 CFR 201.66). This amendment proposes a definition and the option of alternative labeling requirements for
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-21038] 136.
NICEATM in collaboration with the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) announces an independent scientific peer review meeting to evaluate the validation status of five in vitro pyrogenicity test methods: (1) Human PBMC/IL6 in vitro pyrogen test (PBMC/IL6), (2) human whole blood/IL1 in vitro pyrogen
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc E6-21117] 137. Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 6395960 or send an email
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention
[FR Doc E6-21020] 138. Medical Devices Dispute Resolution Panel of the Medical Devices Advisory
The Food and Drug Administration (FDA) is announcing an amendment to the notice of meeting of the Medical Devices Dispute Resolution Panel of the Medical Devices Advisory Committee. This meeting was originally announced in the Federal Register of November 24, 2006 (71 FR 67879). The amendment is being made to reflect a change in the Date and
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-21118] 139. Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 6394766 or send an email
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention
[FR Doc E6-21124] 140. Proposed Data Collections Submitted for Public Comment and Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, the Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention
[FR Doc E6-21125] 141. Proposed Data Collections Submitted for Public Comment and Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, the Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention
[FR Doc E6-21026] 142. Health Professions Preparatory, Health Professions Pregraduate and Indian
Key Dates: Application Deadline: February 28, 2007; Application Review: March 2630, 2007; Application Notification: First week of July, 2007; Award Start Date: August 1, 2007.
I. Funding Opportunity Description
The Indian Health Service (IHS) is committed to encouraging American Indians and Alaska Natives to enter the health professions and
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Indian Health Service
[FR Doc 06-9642] 143. Agency Information Collection Activities: Proposed Collection; Comment
This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) allow the proposed information collection project: ``Pilot Study of Proposed Nursing Home Survey on Resident Safety''. In accordance with the Paperwork Reduction Act of 1995, Public Law 10413 (44
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Agency for Healthcare Research and Quality
[FR Doc 06-9643] 144. Agency Information Collection Activities: Proposed Collection; Comment
This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) allow the proposed information collection project: ``Development of an Electronic System for Reporting Medication Errors and Adverse Drug Events in Primary Care Practice (MEADERS).'' In accordance
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Agency for Healthcare Research and Quality
[FR Doc E6-21028] 145. Government-Owned Inventions; Availability for Licensing
The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federallyfunded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc E6-21029] 146. Government-Owned Inventions; Availability for Licensing
The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federallyfunded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc E6-21037] 147. Government-Owned Inventions; Availability for Licensing
The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federallyfunded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc 06-9631] 148. National Library of Medicine; Notice of Meeting
Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of the following meeting.
The meeting will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health
[FR Doc E6-21021] 149. New Animal Drugs For Use in Animal Feeds; Tylosin
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Elanco Animal Health, A Division of Eli Lilly & Co. The supplemental NADA provides for an alternate feeding regimen for tylosin phosphate in Type C medicated swine feeds used for the
Published: 2006-12-12 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration
[FR Doc E6-20989] 150. National Advisory Council on the National Health Service Corps; Notice of
In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92463), notice is hereby given of the following meeting:
Name: National Advisory Council on the National Health Service Corps
Dates and Times: January 4, 2007, 9 a.m.5 p.m.; January 5, 2007, 9 a.m.5 p.m.; and January 6, 2007, 9 a.m.5 p.m.
Place:
Published: 2006-12-11 DEPARTMENT OF HEALTH AND HUMAN SERVICES : Health Resources and Services Administration
Years: 20002001200220032004200520062007200820092010201120122013