Documents > food and drug administration


Drug and Device Product Approvals

GovernmentDocs 5/5/2008 | 0 (0) | 29 | 0 | 0 | English

FDA DRUG AND DEVICE PRODUCT APPROVALS Volume 17 (1) January 1994 Center for Drug Evaluation and Research *George R. Scott (301) 443-3910 Center for Biologics Evaluation and Research Joseph Wilczek (301) 594-2012 *To whom general inquiries should be directed. This report is compiled by the Division of Drug Information Resources, OM, CDER. It is ava ...  more>>

Review of the Annual Reporting Process for Investigational New Drugs Regulated by the Food and Drug Administration's Center for Biologics Evaluation and Research, A-15-96-50001

HHS 6/19/2008 | 0 (0) | 10 | 0 | 0 | English

‘“ “ . ‘* 4 JUL I 7 Memorandum June Gibbs Brown &L-Inspector General &” Review of the Annual Reporting Process for Investigational New Drugs Regulated by the Food and Drug Administration’s Center for Biologics Evaluation and Research (CIN: A-15-96-50001) Michael A. Friedman, M.D. Lead Deputy Commissioner Food and Drug Administration The attached  ...  more>>

Food and Drug Administration Final Rule Federal Register August C35

FDADocs 5/9/2008 | 0 (0) | 17 | 0 | 0 | English

WAIS Document Retrieval [Federal Register: August-l, 1996 (Volume 61, Number 149)J les and Regulations] age 40153-401553 From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:frOlau96-81 ___--_----------------------------------------------------------------___-----------------_____1______I____c__---------------------------- ...  more>>

Public Health Service Food and Drug Administration Rockville

FDADocs 5/5/2008 | 0 (0) | 20 | 0 | 0 | English

Public Health Service Food and Drug Administration Rockville MD 20857 August 30, 2001 Wayne L. Whittingham AA1 International 2320 Scientific Park Drive Suite 229 Wilmington, NC 28403 . Dear Mr. Whittingham: Your petition requesting the Food and Drug Administration to change the dosage strength of Azathioprine Tablets USP (Imuran), from 50 mg  ...  more>>

Review of the Food and Drug Administration's Cost Increase for the Arkansas Regional Laboratory, A-15-98-50002

HHS 6/19/2008 | 0 (0) | 9 | 0 | 0 | English

DEPARTMENT OF HEALTH & HUMAN SERVICES Office of Inspector General . Memorandum SEP - I 1999 Deputy Inspector General for Audit Services Review of the Food and Drug Administration’s Cost Increasefor the Arkansas Regional Laboratory (CIN: A-15-98-50002) JaneE. Henney, M.D. Commissioner Food and Drug Administration The attachedfi ...  more>>

ADMINISTRATION FOR CHILDREN AND FAMILIES

CMMSdocs 6/30/2008 | 0 (0) | 14 | 0 | 0 | English

ADMINISTRATION FOR CHILDREN AND FAMILIES Senate Committee Report Excerpts from the Departments of Labor, Health and Human Services, and Education, and Related Agencies Appropriation Bill, 2006 (Report No. 109-103) TITLE II--DEPARTMENT OF HEALTH AND HUMAN SERVICES ***************** ADMINISTRATION FOR CHILDREN AND FAMILIES PAYMENTS TO STATES FOR CH ...  more>>

Office of Food Additive Safety

GovernmentDocs 5/5/2008 | 0 (0) | 37 | 0 | 0 | English

DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION CENTER FOR FOOD SAFETY AND APPLIED NUTRITION OFFICE OF OPERATIONS OFFICE OF FOOD ADDITIVE SAFETY OFFICE OF THE DIRECTOR DIRECTOR Laura M. Tarantino, Ph.D. DEPUTY DIRECTOR George H. Pauli, Ph.D. (DBFBC) DIVISION OF PETITION REVIEW DIVISION OF CHEMISTRY RESEARCH AND ENVIRONMENTAL  ...  more>>

PBM Drug Monograph Template

mimama 11/16/2008 | 0 (0) | 0 | 0 | 0 | English

Review of the Food and Drug Administration's Citizen Petition Process, A-15-97-50002

HHS 6/19/2008 | 0 (0) | 11 | 0 | 0 | English

DEPARTME NT HEALTH HUMAN SERVICES off ice of Inspector General I7 Date From Memorandum Subject June Gibbs Brow 236 Inspector Gener -e Review of the Food and Drug Administration’s Citizen Petition Process (CIN: A-15-97-50002) Michael A. Friedman, M.D. Lead Deputy Commissioner Food and Drug Administration The attached final report provides you ...  more>>

Federal Register Notice Volume Number Department of Health and Human Services Food and Drug Administration CFR Part Docket No N RIN AA Use of Ozone Depleting Substances Essential Use Determinatin

FDADocs 5/9/2008 | 0 (0) | 17 | 0 | 0 | English

48370 Federal Register / Vol. 67, No. 142 / Wednesday, July 24, 2002 / Rules and Regulations the purity of the compound in the imported material is shown by satisfactory analysis, that purity, converted to a decimal equivalent of the percentage, is multiplied against the entered amount of the material to establish the amount of pure compound. The  ...  more>>

Public Health Service Food and Drug Administration Rockville 9/17

FDADocs 5/5/2008 | 0 (0) | 21 | 0 | 0 | English

Public Health Service Food and Drug Administration Rockville MD 20857 September 17, 2001 CarllDavid D'Ruiz, MPH Ciba Specialty Chemicals Corporation 4090 Premier Drive P.O. Box 2444 High Point, NC 27261-2444 Dear Dr. D'Ruiz: Your petition requesting the Food and Drug Administration to re-open the administrative record to allow for the submiss ...  more>>

Food and Drug Administration HHS Federal Register North

FDADocs 5/9/2008 | 0 (0) | 22 | 0 | 0 | English

Food and Drug Administration, HHS Federal Register, 800 North Capitol St. NW., suite 700, Washington, DC. (3) The reduced minerals whey shall be derived from milk that has been pasteurized, or the reduced minerals whey shall be subjected to pasteurization techniques or its equivalent before use in food. (c) The reduced minerals whey may be used in  ...  more>>

Office of Food Additive Safety

GovernmentDocs 5/5/2008 | 0 (0) | 51 | 0 | 0 | English

DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION CENTER FOR FOOD SAFETY AND APPLIED NUTRITION OFFICE OF OPERATIONS OFFICE OF FOOD ADDITIVE SAFETY OFFICE OF THE DIRECTOR DIRECTOR Laura M. Tarantino, Ph.D. DEPUTY DIRECTOR George H. Pauli, Ph.D. (DBFBC) DIVISION OF PETITION REVIEW DIVISION OF CHEMISTRY RESEARCH AND ENVIRONMENTAL  ...  more>>

Rules and Regulations Federal Register Vol No Thursday FEDERAL REGISTER Applications for Food and Drug Administration Application Approval to Market a New Drug; Revision of Postmarketing Reporting Req

FDADocs 5/9/2008 | 0 (0) | 21 | 0 | 0 | English

58993 Rules and Regulations Federal Register Vol. 72, No. 201 Thursday, October 18, 2007 This section of the FEDERAL REGISTER contains regulatory documents having general applicability and legal effect, most of which are keyed to and codified in the Code of Federal Regulations, which is published under 50 titles pursuant to 44 U.S.C. 1510. The C ...  more>>


   
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