Bioequivalence - PDFSEARCH.IO - Document Search Engine

Bioequivalence
Results: 910

#	Item
821	FOOD AND DRUG ADMINISTRATION PROGRAM[removed] Add to Reading List Source URL: www.fda.gov Language: English Research Pharmacology Food and Drug Administration Drug safety Bioequivalence Abbreviated New Drug Application Generic drug Clinical trial Clinical site Clinical research Pharmaceutical industry Pharmaceutical sciences
822	“Reporting Information Regarding Falsification of Data” Proposed Rule Add to Reading List Source URL: www.fda.gov Language: English Pharmacokinetics Drug discovery Pharmaceutical industry Clinical research Clinical pharmacology Bioavailability Pre-clinical development Bioequivalence Drug development Pharmaceutical sciences Pharmacology Pharmaceutics
823	Guidance for Industry Handling and Retention of BA and BE Testing Samples U.S. Department of Health and Human Services Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Design of experiments Evaluation methods Clinical trial Pharmaceutical industry Bioequivalence Food and Drug Administration Pharmaceutical sciences Research Clinical research
824	“Reporting Information Regarding Falsification of Data” Proposed Rule Add to Reading List Source URL: www.fda.gov Language: English Medicinal chemistry Drug discovery Pharmaceutical industry Bioavailability Clinical pharmacology Drug development Bioequivalence Pharmacodynamics Food and Drug Administration Pharmaceutical sciences Pharmacology Pharmacokinetics
825	[removed]Federal Register / Vol. 67, No[removed]Thursday, December 19, [removed]Rules and Regulations (ii) One or more construction contracts (includes any contract Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-12-19 06:08:51 Pharmacokinetics Pharmaceutical industry Pharmaceuticals policy Clinical research Abbreviated New Drug Application Bioequivalence Food and Drug Administration Generic drug Drug Price Competition and Patent Term Restoration Act Pharmaceutical sciences Pharmacology Pharmaceutics
826	Generic Drugs Robert L. West Deputy Director Office of Generic Drugs 1 Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceutical industry Clinical pharmacology Generic drug Public domain Abbreviated New Drug Application Bioequivalence Food and Drug Administration Medical prescription Pharmaceutical sciences Pharmacology Pharmaceuticals policy
827	Consumer Health Information www.fda.gov/consumer Generic Drugs: Same Medicine, Lower Cost P Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceutical industry Pharmaceuticals policy Generic drug Public domain Abbreviated New Drug Application Bioequivalence Bupropion MedWatch Pharmacology Food and Drug Administration Pharmaceutical sciences
828	“Reporting Information Regarding Falsification of Data” Proposed Rule Add to Reading List Source URL: www.fda.gov Language: English Research Drug discovery Pharmacokinetics Pharmaceutical industry Clinical trial Dose Nonclinical studies Bioequivalence Bioavailability Pharmacology Pharmaceutical sciences Clinical research
829	N21449S011 Pediatric Clinpharm Review Add to Reading List Source URL: www.fda.gov Language: English Purines Organic chemistry Adefovir Hepatitis B Bioequivalence Bioavailability Nitazoxanide Chemistry Pharmacology Pharmacokinetics
830	Generic Drug User Fee Amendment (GDUFA) SPL Industry Technical Specification Information Electronic Self‐Identification of Generic Drug Facilities or Sites Add to Reading List Source URL: www.fda.gov Language: English Bioequivalence Pharmacokinetics Generic drug Abbreviated New Drug Application Food and Drug Administration Structured Product Labeling Pharmaceutical industry Pharmaceutical sciences Pharmacology Clinical research

UPDATE