Download or read book Laboratory Manual of Pharmaceutical Analysis B Pharm 1st Semester As Per PCI syllabus written by Abhijeet Ojha, Pallavi Pandey, Arun Kumar Singh, Kirti Singh, Anuj Nautiyal, Bhavna and published by Shashwat Publication. This book was released on 2024-02-27 with total page 105 pages. Available in PDF, EPUB and Kindle. Book excerpt: Welcome to the experimental world of Pharmaceutical Analysis. This practical book has been carefully drafted to provide you with a solid foundation in the experimental concepts and basic fundamental in this field. Lab experiments are categorized according to type of titration or technique. Each technique is introduced before experiments. In most of the labs experiments molar and Normal solution are used as followed in recent edition of Indian Pharmacopoeia. Question are presented throughout each experiment. It is important for the students to answer each questions as it will help to improve understanding about experiments. This practical book is the outcome of numerous efforts of authors to incorporate the practical knowledge of Pharmaceutical Analysis. Which has been a requirement of curricula of Pharmacy council of India. This book comprises with 19 Practical’s with short notes as well as viva questions.
Download or read book A Practical Manual of Pharmaceutical Organic Chemistry I As Per PCI Syllabus B Pharm 2nd Semester written by Pynshailang Dkhar and published by Booksclinic Publishing. This book was released on 2022-06-30 with total page 72 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book INSTRUMENTAL METHODS OF ANALYSIS LAB MANUAL written by Raj K. Prasad and published by BookRix. This book was released on 2021-02-06 with total page 38 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book belong to Pharmaceutical analysis practical lab manual based on PCI syllabus which are highly useful for pharmacy under graduate 7th semester student. Its includes a brief description of why the experiment is being performed. Hypothesis: Provide a statement or two about the anticipated outcome of the experiment and a step-by-step description of the experiment including the chemicals, equipment, and/or methods used.
Download or read book Pharmaceutics I written by Dr. P. V. Kasture and published by Pragati Books Pvt. Ltd.. This book was released on 2008-08-07 with total page 284 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Analysis I Practical written by Mrs. Sonali Sheorey & Ms. Meera Honrao and published by . This book was released on 2008 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Topics 1. Introduction 2. Calibration Of Volumetric Apparatus 3. Preparation And Standardisation Of Standard Solutions 4. Indicators 5. Neutralisation Titrations 6. Non-Aqueous Titrations 7. Oxidation-Reduction Titrations 8. Precipitation Titrations 9. Complexometric Titrations 10. Special Category Of Volumetric Methods Of Analysis 11. Gravimetric Analysis
Download or read book Indian Pharmacopoeia 2010 written by Government of India. Ministry of Health & Family Welfare and published by . This book was released on 2010 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Practical Medicinal Chemistry written by Jayaveera K.N./ Subramanyam S. & Reddy, Yogananda K. and published by S. Chand Publishing. This book was released on with total page 166 pages. Available in PDF, EPUB and Kindle. Book excerpt: Introduction 2. Synthesis Of Some Official Medicinal Compounds 3. Assay Of Some Official Compounds 4. Monograph Analysis Of The Following Compounds 5. Identification And Estimation Of Drug Metabolites From Biological Fluids 6. Determination Of Partition Coefficient Of Compounds For Qsar Analysis 7. I.R. Spectra Of Some Official Medicinal Compounds
Download or read book Plant Systematics written by Arun K. Pandey and published by CRC Press. This book was released on 2021-05-31 with total page 340 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is designed to introduce the fundamentals of systematics in a simple, concise and balanced manner. The book aims to equip the students with the basics of plant taxonomy and at the same time also update them with the most recent advances in the field of plant systematics. The book has been organized into 21 chapters that introduce and explain different concepts in a stimulating manner. The text is supplemented with relevant illustrations and photographs. Relevant literature has been added to provide a better picture of the most recent updates in the field of plant systematics. Note: T&F does not sell or distribute the Hardback in India, Pakistan, Nepal, Bhutan, Bangladesh and Sri Lanka.
Download or read book Development and Validation of Analytical Methods written by Christopher M. Riley and published by Elsevier. This book was released on 1996-05-29 with total page 363 pages. Available in PDF, EPUB and Kindle. Book excerpt: The need to validate an analytical or bioanalytical method is encountered by analysts in the pharmaceutical industry on an almost daily basis, because adequately validated methods are a necessity for approvable regulatory filings. What constitutes a validated method, however, is subject to analyst interpretation because there is no universally accepted industry practice for assay validation. This book is intended to serve as a guide to the analyst in terms of the issues and parameters that must be considered in the development and validation of analytical methods. In addition to the critical issues surrounding method validation, this book also deals with other related factors such as method development, data acquisition, automation, cleaning validation and regulatory considerations. The book is divided into three parts. Part One, comprising two chapters, looks at some of the basic concepts of method validation. Chapter 1 discusses the general concept of validation and its role in the process of transferring methods from laboratory to laboratory. Chapter 2 looks at some of the critical parameters included in a validation program and the various statistical treatments given to these parameters.Part Two (Chapters 3, 4 and 5) of the book focuses on the regulatory perspective of analytical validation. Chapter 3 discusses in some detail how validation is treated by various regulatory agencies around the world, including the United States, Canada, the European Community, Australia and Japan. This chapter also discusses the International Conference on Harmonization (ICH) treatment of assay validation. Chapters 4 and 5 cover the issues and various perspectives of the recent United States vs. Barr Laboratories Inc. case involving the retesting of samples. Part Three (Chapters 6 - 12) covers the development and validation of various analytical components of the pharmaceutical product development process. This part of the book contains specific chapters dedicated to bulk drug substances and finished products, dissolution studies, robotics and automated workstations, biotechnology products, biological samples, analytical methods for cleaning procedures and computer systems and computer-aided validation. Each chapter goes into some detail describing the critical development and related validation considerations for each topic.This book is not intended to be a practical description of the analytical validation process, but more of a guide to the critical parameters and considerations that must be attended to in a pharmaceutical development program. Despite the existence of numerous guidelines including the recent attempts by the ICH to be implemented in 1998, the practical part of assay validation will always remain, to a certain extent, a matter of the personal preference of the analyst or company. Nevertheless, this book brings together the perspectives of several experts having extensive experience in different capacities in the pharmaceutical industry in an attempt to bring some consistency to analytical method development and validation.
Download or read book Money Man written by Abhijeet Singh and published by Notion Press. This book was released on 2017-01-19 with total page 231 pages. Available in PDF, EPUB and Kindle. Book excerpt: ""I want a helicopter on the roof; will you get that for me?” she said. ""Which chopper?” the stranger queried without an ounce of doubt. Bhavna was on an ‘accidental date’, with a stranger she just met. She embarked on a journey with this stranger, around the world and to its baffling reality, hidden behind the facade of cosmetic speeches scripted for International Forums. Their journey is marred with experiences that leave them with questions like, ""Is there any space on this planet where money doesn't have control? What really helps to run this world, Hope or Greed?"
Download or read book Handbook of Modern Pharmaceutical Analysis written by Satinder Ahuja and published by Academic Press. This book was released on 2010-11-11 with total page 604 pages. Available in PDF, EPUB and Kindle. Book excerpt: Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. - Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it - Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations - Features detailed coverage of QA, ethics, and regulatory guidance (quality by design, good manufacturing practice), as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS
Download or read book Practical Manual of PHARMACEUTICS II written by G. D. Gupta and published by . This book was released on 2020-02 with total page 226 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Jurisprudence written by Dr. B. S. Kuchekar and published by Pragati Books Pvt. Ltd.. This book was released on 2008-01-08 with total page 152 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book PHARMACEUTICAL INORGANIC CHEMISTRY Simplified Practical Book written by K. S. Jain and published by . This book was released on 2020-02 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Modern Pharmaceutics written by Gilbert S. Banker and published by CRC Press. This book was released on 2002-05-24 with total page 1255 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Completely revised and expanded throughout. Presents a comprehensive integrated, sequenced approach to drug dosage formulation, design, and evaluation. Indentifies the pharmacodynamic and physicochemical factors influencing drug action through various routes of administration."
Download or read book Pharmaceutical Organic Chemistry written by and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Vogels Textbook Of Quantitative Chemical Analysis written by Mendham and published by Pearson Education India. This book was released on 2006-02 with total page 838 pages. Available in PDF, EPUB and Kindle. Book excerpt:
