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Bioequivalence
Results: 910

#	Item
621	FOOD AND DRUG ADMINISTRATION (FDA) Center for Drug Evaluation and Research (CDER) Advisory Committee for Pharmaceutical Science and Clinical Pharmacology (ACPS-CP) Hilton Washington D.C./Silver Spring Silver Spring, MD Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Pharmaceuticals policy Bioequivalence Center for Drug Evaluation and Research Generic drug Dermatologic and Ophthalmic Drugs Advisory Committee Pharmaceutical sciences Pharmacology Food and Drug Administration
622	[removed]Federal Register / Vol. 62, No[removed]Tuesday, December 30, [removed]Notices physically or chemically interact with a drug substance. Altered BA of drug Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Clinical research Pharmaceutical industry Food and Drug Administration Bioequivalence Abbreviated New Drug Application Generic drug Bioavailability New Drug Application Pharmaceutical sciences Pharmacology Pharmacokinetics
623	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Clinical research Bioequivalence Pharmacokinetics Center for Drug Evaluation and Research Pharmaceutical sciences Pharmacology Food and Drug Administration
624	Bioequivalence Studies - Figure 2a Add to Reading List Source URL: www.fda.gov
625	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Therapeutics United States Public Health Service Bioequivalence Center for Drug Evaluation and Research 12-hour clock Pharmaceutical sciences Pharmacology Clinical research
626	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Pharmacokinetics Clinical pharmacology Food and Drug Administration Bioequivalence Generic drug Abbreviated New Drug Application Center for Drug Evaluation and Research Drug discovery Orlistat Pharmaceutical sciences Pharmacology Clinical research
627	GDUF Negotiations Meeting[removed]PUBLIC Minutes Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Research Clinical research Pharmaceuticals policy Center for Drug Evaluation and Research Generic drug Bioequivalence Abbreviated New Drug Application New Drug Application Food and Drug Administration Pharmaceutical sciences Pharmacology
628	Bioequivalence Studies Figure 1B Add to Reading List Source URL: www.fda.gov
629	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Clinical pharmacology Therapeutics Bioequivalence Center for Drug Evaluation and Research Drug discovery Dermatologic and Ophthalmic Drugs Advisory Committee Oncology Drug Advisory Committee Pharmaceutical sciences Pharmacology Food and Drug Administration
630	J:licationsrmaceutical Sciences Q&Aking copyqa_sp_qr_e.wpd Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:26:03 Clinical research Pharmacokinetics Pharmaceuticals policy Drug Master File Bioequivalence Validation Abbreviated New Drug Application Good manufacturing practice Food and Drug Administration Pharmaceutical sciences Pharmacology Pharmaceutical industry

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