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

1. Pediatrics pharmacology Dr.Azad Abduljabar Haleem [email protected] 2. • • • • • • • •Childhood: 0 – 18 years Neonate: 28 days Infant: 1st year Toddlers:…

1. Pharmacology Rosalie C. Villora MSN, RN 2. Objectives Identify principles of pharmacology that relate to nursing care. Explain absorption, excretion, desired effect. Describe…

Slide 1BIOPHARMACEUTICAL CONSIDERATION IN DRUG PRODUCT DESIGN By Sarafadeen Adebayo, Ph.D. Slide 2 Slide 3 DEVELOPING DRUG DELIVERY SYSTEM THAT HIT A DESIRED TARGET PHARMACOKINETIC…

Slide 1Dissolution Testing of Immediate Release Products The goal of dissolution testing is to assure the pharmaceutical quality: – The ability to manufacture the product…

1. MED factsPOCKET GUIDE OF DRUG INTERACTIONS Second Edition MED factsPOCKET GUIDE OF DRUG INTERACTIONS Second Edition Provided as an Educational Service by Provided as an…

1. BIOPHARMACEUTICSBYNILIMANKA DASASSISTANT PROFESSORRIPSAT, AGARTALA, TRIPURA 2. Introduction of Biopharmaceutics:Biopharmaceutics:Study of physicochemical properties ofdrugs…

ABSORPTION OF DRUG Submitted To Dr. Santa Raj Joshi Department of Pharmacy School of Science Kathmandu University Submitted By Feb 2008 Table of Content Anana Sharmat Deep…

Introduction Bioavailability is defined as rate and extent of absorption of unchanged drug from it’s dosage form and become available at the site of action. Bioavailability…

www.wjpps.com Vol 3, Issue 3, 2014. 1393 D.Lohithasu et al. World Journal of Pharmacy and Pharmaceutical Sciences FORMULATION AND CHARACTERIZATION OF PIROXICAM LIQUISOLID…