bioequivalence study sustained release tablets de saurabh rekha (5 résultats)

Taschenbuch. Etat : Neu. Bioequivalence Study of Sustained-Release Tablets | Rekha Singh Saurabh (u. a.) | Taschenbuch | 80 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659551925 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -A generic drug (generic drugs, short: generics) is a drug which is produced and distributed without patent protection. The generic drug may still have a patent on the formulation but not on the active ingredient. Based on clinical, pharmacokinetic and statistical data obtained from 18 subjects normal, adult, human subjects under fasting conditions, it was concluded that both the formulations were well tolerated following a single dose administration of the investigational product and test formulation was found to be bioequivalent to the reference formulation the 90% confidence intervals for the means of the primary efficacy variables; AUC0-t,Cmax and AUC0- determined. 80 pp. Englisch.

Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Saurabh Rekha SinghMs.Rekha Singh Saurabh did her B.Pharm. and M.Pharm. (Pharmacology) from BN Institute of Pharmaceutical Sciences, Udaipur,affiliated to RUHS, jaipur. Her preferred area of research is in clinical research, diabetes.

Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -A generic drug (generic drugs, short: generics) is a drug which is produced and distributed without patent protection. The generic drug may still have a patent on the formulation but not on the active ingredient. Based on clinical, pharmacokinetic and statistical data obtained from 18 subjects normal, adult, human subjects under fasting conditions, it was concluded that both the formulations were well tolerated following a single dose administration of the investigational product and test formulation was found to be bioequivalent to the reference formulation the 90% confidence intervals for the means of the primary efficacy variables; AUC0-t,Cmax and AUC0- ¿ determined.Books on Demand GmbH, Überseering 33, 22297 Hamburg 80 pp. Englisch.

Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - A generic drug (generic drugs, short: generics) is a drug which is produced and distributed without patent protection. The generic drug may still have a patent on the formulation but not on the active ingredient. Based on clinical, pharmacokinetic and statistical data obtained from 18 subjects normal, adult, human subjects under fasting conditions, it was concluded that both the formulations were well tolerated following a single dose administration of the investigational product and test formulation was found to be bioequivalent to the reference formulation the 90% confidence intervals for the means of the primary efficacy variables; AUC0-t,Cmax and AUC0- determined.