The Pharmacy Council of India's (PCI) revised B. Pharmacy syllabus is followed in this state-of-the-art book. The broader topics of pharmaceutical quality assurance that undergrads, postgrads, industry professionals, researchers, and students getting ready for different competitive tests need to be covered in this book's encompassing content. The writing style of this book is clear, straightforward, and uncomplicated, which sets it apart from others. For the self-evolution of learning, the book is complemented by questions in the formats of multiple choice, fill in the blank, true-false, short answer, and long answer. Additionally included are the solutions to the True-False, Fill in the Blank, and Multiple-Choice problems. Links to websites and recommended reading are provided to assist readers in staying up to date on the most recent advancements in the field of pharmaceutical quality assurance. The book can be used as the main source of instruction or as supplementary material by academicians and teachers at universities and colleges for undergraduate and graduate pharmacy courses.

This Quality Assurance book intended for Pharmacy students especially Third year students of Bachelor of Pharmacy. This book is also beneficial for professionals engaged in Quality Assurance Department. We have tried to emphasize on the basics of Quality Assurance. Thus complexity of the matter has been avoided with a view that complete course content has to be completed by the student in limited time period. This book present a concise and effective reference to the topics with an approach to make it interesting and convenient to remember the complicated Quality Assurance terms.

Industrial Pharmacy is the science of manufacturing, development, marketing and distribution of drug products, including quality assurance of the developed drug formulation. This book covers all topics required by students of Pharmacy. Industrial Pharmacy: A textbook is divided into two parts, ‘Industrial Pharmacy’ Part-I explains the formulation, manufacture, and quality control of tablets, capsules, parenteral dosage forms, liquid orals, ophthalmic dosage form and aerosols. In addition, topics such as ‘Pre-formulation’, ‘Cosmetics’ and ‘Packaging Material Science’ have also been briefly discussed. Part-II has been designed with the objective of imparting knowledge of the pilot plant scaleup considerations of different dosage forms. The students will be able to understand the technology transfer process from R&D to production with the necessary documentation. This book also provides information about drug regulations, roles and responsibilities of drug regulatory requirements such as ANDA and NDA, QMS.

Introducing the book "Industrial Pharmacy-II" is something that fills me with an incredible amount of joy. The content of this book has been meticulously crafted to adhere to the curriculum for Bachelor of Pharmacy students that has been outlined by the Pharmacy Council of India. An effort has been made to investigate the topic using terminology that is as straightforward as possible in order to make it more simply digestible for pupils. The book has a number of illustrations, such as flowcharts and diagrams that make it simple for students to comprehend complex ideas. It is the author's honest desire that both students and academicians would take something helpful away from reading this book.

The study of elements and the compounds they form is referred to as inorganic chemistry. Organic chemistry, on the other hand, is concerned with carbon and the compounds it forms. However, there is a lot of crossovers between organic and inorganic, thus the two categories are not completely separate from one another. The book's key features include an overview of general elements and the relevance of those aspects, with a focus on the applications in the pharmaceutical field. is a standard textbook that is often used for an introductory level inorganic chemistry undergraduate course. It provides a complete pedagogical framework to assist students with understanding essential concepts. This book gives a decent introduction to the topic; explains a variety of inorganic compounds as well as the minimal chemical facts and ideas that are required to comprehend current inorganic chemistry; offers a good overview of the subject. provides an advanced and in-depth descriptive treatment of all of the official compounds featured, with a significant emphasis on the production, characteristics, assay, and medicinal uses of the compounds. The book “A Textbook of Pharmaceutical Inorganic Chemistry” is prepared in an exhaustive fashion and includes facts that have been brought up to date about the subjects that are covered in the curriculum. The book Covers the fundamentals of basic inorganic chemistry that are necessary for undergraduate pharmacy students, while students of chemistry, biology, and other relevant subjects will also find this book to be fascinating and informative.

This book structured in TWO different parts. These parts are as follows: Part I emphasizes on GCP (Good Clinical Practices), GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), USFDA-NDA/ANDA (U S Food and Drug Administrations- New Drug Approval/Abbreviated New Drug Approval) and TQM (Total Quality Management). GCP (Good Clinical Practices) is an international quality standard that is provided by International Conference on Harmonization (ICH), an international body that defines standards, which governments can transpose into regulations for clinical trials involving human subjects. Good Clinical Practice guidelines include protection of human rights as a subject in clinical trial. It also provides assurance of the safety and efficacy of the newly developed compounds. Good Clinical Practice Guidelines include standards on how clinical trials should be conducted, define the roles and responsibilities of clinical trial sponsors, clinical research investigators, and monitors. In the pharmaceutical industry monitors are often called Clinical Research Associates. GLP (Good Laboratory Practices) deals with the organization, process and conditions under which laboratory studies are planned, performed, monitored, recorded and reported. GLP practices are intended to promote the quality and validity of test data. Published GLP regulations and guidelines have a significant impact on the daily operation of an analytical laboratory. GMP (Good Manufacturing Practices) Manufacturing relies on the ability to reproduce exactly a single product hundreds, if not thousands, of times. To make this possible, guidelines have been drawn up in most countries that are similar to the FDA ones described here that define GMPs. Diagnostic companies, including those manufacturing and distributing biosensors, cannot sell their products for either public or professional use unless they have been approved on the basis of these guidelines. USFDA-NDA/ANDA (U S Food and Drug Ad

It is with great pleasure that we introduce the book “Pharmaceutics-I”. The book allows for the lucid understanding of different dosage forms and processing methods. This book is a genuine effort to clarify the basics of Pharmaceutics in an effortless and interesting manner, as per the syllabus prescribed for the D. Pharm, Part I students by Board of Technical Education. All efforts have been made to keep the text error-free and to present the subject in a student friendly and easy to understand. However, any suggestions and constructive comments would be highly appreciated and incorporated in the future edition.

The titled book is A Textbook of PHARMACEUTICAL INORGANIC CHEMISTRY (Theory) (As per PCI regulation). The idea of book originated by authors to convey a combined database for easy understanding of PHARMACEUTICAL INORGANIC CHEMISTRY (Theory). This book is intended to communicate information on inorganic chemistry, to direct tutors and learners regarding fundamental concepts in PHARMACEUTICAL INORGANIC CHEMISTRY (Theory). The major aim to write this textbook is to provide information in articulate summarized manner to accomplish necessities of undergraduates as per PCI regulation. This volume is designed not only according to curriculum of undergraduate courses in pharmacy by PCI but also to communicate knowledge on Pharmaceutical Jurisprudence for post graduate learners. We assured this book will be originated very valuable by graduates, post graduates, professors and industrial learners. However any suggestion for further improvement of text are welcome and will be taken due note of.

"This book describes what constitutes modern pharmaceutical analysis and coveres the topics in very simplified language, which is easy to understand. This book would be invaluable for students, researchers, and industry professionals. Coverage of various topics is comprehensive encompassing the newly implemented PCI syllabus for postgraduate and undergraduate courses and will be of particular interest as a reference text for research students of pharmaceutical sciences as well. This book is intended to expose the readers to theoretical basis, instrumentation aspects and applications of modern analytical techniques. "