Integrated high capacity solid phase extraction-MS/MS system for pharmaceutical profiling in drug discovery
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Automated Microbial Identification: A Comparison of USP and EP Approaches
Pharma Live, , Analytical Discussion, 0
Introduction Microbial identification places an important role in pharmaceutical processing. Microbial identification can be defined as “microbial characterization by a...
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A Generic UHPLC-UV-MS Method for Cleaning Verification of Highly Potent Drugs
Pharma Live, , Analytical Discussion, 0
Abstract Cleaning validation (CV) is a Good Manufacturing Practices (GMP) requirement in the manufacturing of drug substances and drug...
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API Characterization for a Speedy and Successful Formulation Strategy
Pharma Live, , Analytical Discussion, 0
The physicochemical properties of the API in a solid state are extremely important as they affect the choice and...
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Absorption and Drug Development: Solubility, Permeability, and Charge State, 2nd Edition
Pharma Live, , Analytical Discussion, 0
With this book as their guide, readers have access to all the current information needed to thoroughly investigate and...
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Solid Dosage and Excipients 2015 eBook – Courtesy (PharmTech)
Pharma Live, , Analytical Discussion, 0
Pharmaceutical Technology‘s 2015 Solid Dosage and Excipients eBook examines how advances in technology, equipment, excipients, analytical techniques, software, and...
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Biorelevant dissolution media as a predictive tool for glyburide a class II drug – ScienceDirect Elsevier
Pharma Live, , Analytical Discussion, Uncategorized, 0
This entry was posted in Analytical Discussion and tagged biorelevant, class 2, Dissolution media, glibenclamide, glyburide. The purpose of...
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METHOD VALIDATION OF ANALYTICAL PROCEDURES
Pharma Live, , Analytical Discussion, 0
ABOUT AUTHORSPrakash Chanda GuptaQC Executive,National Healthcare Pvt. Ltd., [email protected] ABSTRACTAfter the development of an analytical procedure, it is must...
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