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User fee
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#	Item
491	GAO[removed]Highlights, DRUG SAFETY: FDA Has Conducted More Foreign Inspections and Begun to Improve Its Information on Foreign Establishments, but More Progress Is Needed Add to Reading List Source URL: www.gao.gov Language: English - Date: 2011-09-29 08:45:25 Health Clinical pharmacology Pharmacology Therapeutics United States Public Health Service Food and Drug Administration Amendments Act Prescription Drug User Fee Act Food and Drug Administration Pharmaceutical sciences Clinical research
492	January 13, 2014 INFORMATIONAL NOTICE TO COMPANIES REPORTING TO THE TREASURY REGARDING USER FEES FOR CALENDAR YEAR 2014 Please be advised that the Department of the Treasury, Financial Management Service, has not changed Add to Reading List Source URL: fiscal.treasury.gov Language: English - Date: 2014-07-17 10:07:21 Investment Building engineering Insurance Sureties Surety bond Reinsurance Maintenance fee Law Financial economics Legal costs Types of insurance
493	Fee Schedule for Reproduction Services • User Agreement form must be completed and approved before an order will be processed • Prepayment of fees is required • Reproduction of a print or negative can take up to 2 Add to Reading List Source URL: www.jewishmuseum.ca Language: English - Date: 2011-05-17 13:44:44 Photograph Mail Compact Disc Electronics Digital media Information science Digital photography Photographer Photography
494	Division of Documents Management Food and Drug Administration[removed]New Hampshire Ave. Bldg. 51, Rm[removed]Silver Spring, MD[removed]Re: Docket No. FDA-2012-N-0967, Prescription Drug User Fee Act PatientFocused Drug Develop Add to Reading List Source URL: www.alsa.org Language: English - Date: 2012-11-01 15:37:20 Pharmaceutical sciences Clinical research Rare diseases Pharmaceuticals policy Amyotrophic lateral sclerosis Motor neurone disease ALS Association Prescription Drug User Fee Act FDA Fast Track Development Program Food and Drug Administration Health Pharmacology
495	Index of Fees This represents examples from each category and is not meant to be an all inclusive list of fees charged on campuses. The Category IV fee list includes common fees, used by most campuses, and should not be Add to Reading List Source URL: www.calstate.edu Language: English - Date: 2013-03-26 14:45:26 Credit Economics Public finance Student fee Business Credit card Non-sufficient funds Late fee User fee Financial economics Fee Pricing
496	Athletics and Recreation Facility Rental/Use Contract This Contract, dated this ________day of ____________________, 20____, is between the University of Alaska, hereafter referred to as “UA” and: User Name:________ Add to Reading List Source URL: www.alaska.edu Language: English - Date: 2014-04-07 14:58:59 Real property law Types of insurance Financial institutions Institutional investors Lease Fee Liability insurance Insurance Law Business Private law
497	BACKGROUND The Federal Food, Drug, and Cosmetic Act (FD&C Act), as amended by the Animal Generic Drug User Fee Act (AGDUFA), authorizes FDA to collect fees from the animal pharmaceutical industry to augment appropriation Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Food and Drug Administration Food law Pharmaceutical industry Generic drug Federal Food Drug and Cosmetic Act Prescription Drug User Fee Act Pharmaceutical sciences Pharmaceuticals policy Health
498	USER FEE OBLIGATIONS User fees are expended only for costs necessary to support the process for the review of abbreviated applications for generic new animal drugs, as defined in AGDUFA. Allowable and excludable costs fo Add to Reading List Source URL: www.fda.gov Language: English Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Abbreviated New Drug Application Pharmaceutical sciences Clinical research Pharmacology
499	EXECUTIVE SUMMARY The Animal Generic Drug User Fee Act (AGDUFA) of 2008 requires the Food and Drug Administration (FDA) to report annually on the financial aspects of its implementation of the Act. Required under AGDUFA, Add to Reading List Source URL: www.fda.gov Language: English Clinical research Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Generic drug Prescription Drug User Fee Act Pharmaceutical sciences Pharmaceuticals policy Pharmacology
500	TOTAL COST OF THE PROCESS FOR THE REVIEW OF ABBREVIATED APPLICATIONS FOR GENERIC NEW ANIMAL DRUGS Table 6 shows the costs for the review of abbreviated applications for generic new animal drugs during the past two fiscal Add to Reading List Source URL: www.fda.gov Language: English Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Pharmaceuticals policy Abbreviated New Drug Application Prescription Drug User Fee Act Pharmaceutical sciences Clinical research Pharmacology

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