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Bøger af Manish Pathak

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  • af Manish Pathak
    368,95 kr.

    This book is for the graduate students of Pharmacy or Chemistry. Books help students to learn about the synthesis of medicinal drugs their assay methods and drawing of chemical structure of medicinal drugs using Chem Draw software. In this book author considers the requirement of synthesis like as chemical and glassware requirement, discussed the principles of reaction with brief theory & simple calculations.

  • af Manish Pathak
    436,95 kr.

    The Practical book is an attempt to give to students of practical Pharmaceutical organic chemistry the benefit of some 11 years of experience in the teaching of the subject. The new procedures and many specialized techniques are incorporated into this book. Furthermore, new experiments for the elementary student have emanated; have been tried out with large classes of undergraduate students over several sessions with gratifying success and have now been included in the present text-book.

  • af Manish Pathak
    500,95 kr.

    The objective of the study IS to develop and validate the dissolution method assisted with the analytical method for the estimation of remogliflozin etabonate. Dissolution test has emerged in the pharmaceutical field as a very important tool to characterize drug product performance. It provides measurements of the bioavailability of a drug as well as demonstrates bioequivalence from batch to batch. Besides, dissolution is a requirement for regulatory approval for product marketing and is a vital component of the overall quality control program, particularly in the pharmaceutical industry; the quality of the drugs produced must be carefully tested in tablets, solutions, suspension, or other dosage forms. Slight differences in composition or in drug purity can affect therapeutic value itself. Newer and better methods for pharmaceuticals are therefore constantly required. Ich q2(r1) guideline entitled ¿validation of analytical procedures: text and methodology ¿requires validation to be carried out of the developed method to ensure that the developed analytical method will consistently produce results meeting predetermined specifications and quality attributes.

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