Bioavailability & Bioequivalence: Regulatory perspectives in generic drug product development Dr B Praveen Reddy Managing Director Riconpharma India Pvt Ltd Hyderabad…

1. Delivery of Biopharmaceuticals Should be addressed during the pre-clinical phase ofthe drug development processThe route by which the drug candidate is delivered or administered…

1. The Application of the Scientific Method:Preclinical Trials Copyright 2010. PEER.tamu.edu 2. What do you think? Have you ever had to take a medicine totreat an illness?…

Slide 1 Slide 2 April 20, 2012 Prague, Czechoslovakia Slide 3 Financial Disclosure I have no relevant financial relationships to disclose. Slide 4 Agenda --- New Structure…

1.Development of Innovative Medicines in Russian Academic Institutes. The Experience of Nonprofit Partnership “Orchemed” Prof. Sergey Bachurin, corresponding-member of…

1.Comparison among validations of twoanalitical methods for the determinationof cidofovir in human plasma“Comparison of the quantitative performancesand measurement uncertainty…

1.   2. INSIDE THE FDA The Business and Politics Behind the DrugsWe Take and the Food We Eat AUTHOR: Fran Hawthorne PUBLISHER: John Wiley & Sons, Inc. DATE OF PUBLICATION:…

1. 1 2. Outline • Overview of computer aided drug designing. • Clinical and Pre-clinical trials. • Prediction of properties and Drug-likeness. • Advanced treatments…

1. Bringing a Drug or Device to Market Public Relations Implications An Overview of the FDA Approval Process 2nd Edition November, 2005 Mark Senak, J.D -– Drugs and Biologics…

1. Tony Pan ,Ashish Sharma, Benjamin Rutt, Metin Gurcan, Stephen Langella, Joel Saltz, Tahsin Kurc Department of Biomedical Informatics The Ohio State University Medical…