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Generic drug
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951	GUIDANCE DOCUMENT FOR INDUSTRY Review of Drug Brand Names Draft Date Revision Date Effective Date Add to Reading List Source URL: www1.webcastcanada.ca Language: English - Date: 2014-03-05 15:46:45 Pharmaceutical industry Food and Drug Administration Clinical research Pharmaceuticals policy Generic drug Abbreviated New Drug Application Drug Identification Number Clinical trial Medical prescription Pharmacology Pharmaceutical sciences Health
952	Revisions to Guidance to Industry 2125fnl.PDF Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Prescription Drug User Fee Act Center for Biologics Evaluation and Research New Drug Application Investigational New Drug FDA Special Protocol Assessment Center for Drug Evaluation and Research Biologic Generic drug Food and Drug Administration Medicine Health
953	APPENDIX A CONDITIONS FOR ASSESSMENT AND USE OF FEES The FD&C Act, as amended by AGDUFA, specifies three legal conditions that must be met each fiscal year for FDA to collect and spend generic new animal drug user fees. Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmaceuticals policy Pharmacology Therapeutics United States Public Health Service Federal Food Drug and Cosmetic Act Appropriation bill Continuing resolution Medicine Pharmaceutical sciences Government
954	Ignoring a solution to chronic drug shortages Original Reporting \| By T.J. Lewan \| Health care, Medicine May 7, 2014 — Since shortages of critical drugs became a fixture of the American medical landscape a decade ago, Add to Reading List Source URL: www.remappingdebate.org Language: English - Date: 2014-05-09 12:54:34 Pharmaceuticals policy Pharmaceutical industry Food and Drug Administration Pharmacy Generic drug Abbreviated New Drug Application Compounding Clinical trial Prescription Drug User Fee Act Pharmaceutical sciences Pharmacology Health
955	MEETING THE LEGAL CONDITIONS FOR USER FEES IN FY 2012 AGDUFA imposes three legal conditions that must be satisfied in each fiscal year before FDA can collect and spend generic new animal drug user fees. A summary of how Add to Reading List Source URL: www.fda.gov Language: English Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Medicinal chemistry Pharmaceutical sciences Pharmacology Clinical research
956	OMB approved # [removed]MEDICAID DRUG UTILIZATION REVIEW ANNUAL REPORT FEDERAL FISCAL YEAR Section[removed]g[removed]D) of the Social Security Act requires each State to submit an annual report on the operation of its Medi Add to Reading List Source URL: www.medicaid.gov Language: English - Date: 2014-10-23 18:40:43 Healthcare reform in the United States Presidency of Lyndon B. Johnson Pharmaceuticals policy Medicaid Medical prescription Pharmacist Medication therapy management Generic drug Disease management Health Medicine Federal assistance in the United States
957	January 22, 2014 Division of Dockets Management (HFA-305) Food and Drug Administration 5600 Fishers Lane, Room 1061 Rockville, MD[removed]Comments of the Patient, Consumer, and Public Health Coalition Add to Reading List Source URL: npalliance.org Language: English - Date: 2014-01-22 21:07:23 Medicine Pharmaceutical industry Food and Drug Administration Drug safety Generic drug New Drug Application Prescription medication Levofloxacin Moxifloxacin Pharmaceutical sciences Pharmacology Pharmaceuticals policy
958	PDF Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-04-25 18:26:40 Pharmaceutical industry Biotechnology Food and Drug Administration Biosimilar Biopharmaceutical New Drug Application Bioequivalence Generic drug Drug Price Competition and Patent Term Restoration Act Pharmaceutical sciences Pharmacology Clinical research
959	Investor Statement on Board Oversight of Biosimilar Issues The pharmaceutical industry represents important investments for our portfolios and important producers of life-altering medicines. We greatly value pharmaceutic Add to Reading List Source URL: freepdfhosting.com Language: English - Date: 2014-08-11 08:46:54 Pharmaceutical industry Biosimilar Biotechnology Drugs Hospira Biologic Food and Drug Administration Generic drug European Medicines Agency Pharmaceutical sciences Pharmacology Clinical research
960	BuchananIngersoll 1776 K Street, Pi W Suite 800 WashIngton. DC[removed] Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-02-08 11:01:09 Pharmacokinetics Cytochrome P450 Ketones Rodenticides Warfarin Oxandrolone CYP2C9 Bioavailability Generic drug Chemistry Pharmacology Pharmaceutical sciences

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