Department of Health and Human Services June 1, 2006 – Federal Register Recent Federal Regulation Documents

Advisory Committee on Immunization Practices: Teleconference
Document Number: E6-8590
Type: Notice
Date: 2006-06-01
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
National Institute for Occupational Safety and Health (NIOSH); Advisory Board on Radiation and Worker Health (ABRWH)
Document Number: E6-8586
Type: Notice
Date: 2006-06-01
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Announcement of Availability of Funds for One Family Planning Clinical Training Cooperative Agreement
Document Number: E6-8458
Type: Notice
Date: 2006-06-01
Agency: Department of Health and Human Services
This announcement seeks applications from public and nonprofit private entities for one cooperative agreement grant to establish and operate one family planning clinical training project to serve Title X service delivery projects nationally. The project will include two components: (1) Training of clinical preceptors to work in Title X family planning service projects; and (2) conducting a national clinical training meeting every other year of the project. In close collaboration with the Office of Family Planning (OFP) project officer, the successful applicant will be responsible for the development and overall management of all components of the clinical training program. The successful applicant should anticipate substantial involvement of the OFP project officer in the conduct of this cooperative agreement.
Proposed Data Collections Submitted for Public Comment and Recommendations
Document Number: E6-8453
Type: Notice
Date: 2006-06-01
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
New Animal Drugs for Use in Animal Feeds; Melengestrol, Ractopamine, Monensin, and Tylosin
Document Number: E6-8420
Type: Rule
Date: 2006-06-01
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an abbreviated new animal drug application (ANADA) filed by Ivy Laboratories, Division of Ivy Animal Health, Inc. The ANADA provides for use of single-ingredient Type A medicated articles containing melengestrol, ractopamine, monensin, and tylosin to make four-way combination drug Type C medicated feeds for heifers fed in confinement for slaughter.
Guidance for Industry on Chemistry, Manufacturing, and Controls Information; Withdrawal and Revision of Seven Guidances
Document Number: E6-8417
Type: Notice
Date: 2006-06-01
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing the withdrawal of five and the revision of two guidances for industry, because some of the principles in these guidances are inconsistent with the agency's initiative, Pharmaceutical Current Good Manufacturing Practices (CGMPs) for the 21st Century (CGMP Initiative). Several of the guidances listed in this notice are cross-Center guidances relating to products regulated by the Center for Drug Evaluation and Research (CDER), the Center for Biologics Evaluation and Research (CBER), and the Center for Veterinary Medicine (CVM).
Request for Public Comment: 60-Day Proposed Information Collection
Document Number: 06-5021
Type: Notice
Date: 2006-06-01
Agency: Department of Health and Human Services, Indian Health Service
The Indian Health Service (IHS), as part of its continuing effort to reduce paperwork and respondent burden, conducts a pre- clearance consultation program to provide the general public and Federal agencies with an opportunity to comment on proposed and/or continuing collections of information in accordance with the Paperwork Reduction Act of 1995 (PRA95) (44 U.S.C. 3506(c)(2)(A)). This program helps to ensure that requested data can be provided in the desired format, reporting burden (time and financial resources) is minimized, collection instruments are clearly understood, and the impact of collection requirements on respondents can be properly assessed. Currently, the IHS is providing a 60-day advance opportunity for public comment on a proposed new collection of information to be submitted to the Office of Management and Budget for review.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.