Investigation and Need of Bioequivalence Study: Methodology and Regulatory Requirement

Publisher： Bentham Science Publishers

ISSN： 2213-476X

Source： Applied Clinical Research, Clinical Trials and Regulatory Affairs, Vol.1, Iss.2, 2014-08, pp. : 93-106

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Current regulatory approaches of bioequivalence testing

By Karalis Vangelis   Macheras Panos  

Expert Opinion on Drug Metabolism and Toxicology, Vol. 8, Iss. 8, 2012-08 ,pp. : 929-942

Informa Healthcare

Access to resources Recommend Favorite

Levothyroxine: therapeutic use and regulatory issues related to bioequivalence

By Wartofsky Leonard  

Expert Opinion on Pharmacotherapy, Vol. 3, Iss. 6, 2002-06 ,pp. : 727-732

Informa Healthcare

Access to resources Recommend Favorite

Investigation of the Structural Requirement for Blocking the Human CCR5 Chemokine Receptor. An Insight from Quantitative Structure Activity Relationships Study

By  

Letters in Drug Design & Discovery, Vol. 6, Iss. 2, 2009-03 ,pp. : 114-124

Bentham Science Publishers

Access to resources Recommend Favorite

A New Approach for Outliers in a Bioavailability/Bioequivalence Study

By Liao Jason J. Z.  

Journal of Biopharmaceutical Statistics, Vol. 17, Iss. 3, 2007-05 ,pp. : 393-405

Taylor & Francis Ltd

Access to resources Recommend Favorite

The impact of stereoisomerism in a bioequivalence study on two formulations of doxepin

By Protheroe R.J.   Johnson P.A.   Midha K.K.   Hubbard J.W.   Rawson M.   Schwede R.  

European Journal of Pharmaceutical Sciences, Vol. 4, Iss. 3, 1996-05 ,pp. : 133-138

Elsevier

Access to resources Recommend Favorite