Download or read book Indian Pharmacopoeia 2007 written by and published by . This book was released on 2007 with total page 264 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Indian Pharmacopoeia 2007 without special title written by and published by . This book was released on 2007 with total page 620 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Innovations in Indian Pharmacopoeia 2007 written by Indian Drug Manufacturers' Association and published by . This book was released on 2007 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt:
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 INDIAN PHARMACOPOEIA 2018 ADDENDUM 2021 written by and published by . This book was released on 2021 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Indian Medicinal Plants written by C.P. Khare and published by Springer Science & Business Media. This book was released on 2008-04-22 with total page 836 pages. Available in PDF, EPUB and Kindle. Book excerpt: In an easy to use dictionary style of A–Z presentation, this volume lists the taxonomy and medicinal usage of Indian plants. Also given are both traditional Indian and international synonyms along with details of the habitats of the plants. This book, illustrated by over 200 full-color figures, is aimed at bringing out an updated Acute Study Dictionary of plant sources of Indian medicine. The text is based on authentic treatises which are the outcome of scientific screening and critical evaluation by eminent scholars. The Dictionary is presented in a user-friendly format, as a compact, handy, easy to use and one-volume reference work.
Download or read book Laboratory Manual of Pharmaceutics written by Dr. Remeth J. Dias and published by Trinity Publishing House, Satara. This book was released on 2023-09-28 with total page 196 pages. Available in PDF, EPUB and Kindle. Book excerpt: We are very pleased to put forth the revised edition of 'Laboratory Manual of Pharmaceutics'. We have incorporated all the suggestions, modified it to make it easier, student friendly and relevant in terms of achieving curriculum outcome. We are very much thankful to all the learned teachers who have given their feedback whole-heartedly. We have even incorporated the changes in this manual based on the feedback given by the teachers from all the institutes. Now, we believe that the manual has been fulfilling the aspirations of pharmaceutics teachers and students too. This manual is prepared as per PCI Education Regulations, 2020 for Diploma Course in Pharmacy. The procedures and formulas of all the experiments are reviewed and added, so that the advancement in the methods or apparatus can be addressed. This manual is designed for 'outcome-based education' and each experiment is arranged in a uniform way such as practical significance, practical outcomes (PrOs) and its mapping with course outcomes, minimum theoretical background, resources used, procedure, precautions, observations, result, conclusion, references and related questions. We have also given the readings for the reference of students and better understanding. Moreover, assessment scheme is also given to help the student and teacher to know what to be assessed. A sincere attempt has been made through this manual to provide practical knowledge to the students related to various topics of Pharmaceutics. The manual mainly includes the experiments through which the students will learn to prepare conventional dosage forms and few cosmetic formulations in the laboratory. Besides, experiments related to handling of Indian Pharmacopoeia and National formulary of India will make the students familiar with the Indian official compendiums. The demonstration based experiments will help the students to understand the tablet compression process and quality control test of tablets, capsules, emulsions and single-dose parenteral preparations. A brief introduction to various dosage forms before the related experiments can assist in better perception of the experiment. Each experiment is divided into sections like aim, practical significance, relevant professional competencies, relevant course outcomes, practical skills, relevant affective domain related outcomes, practical outcomes, minimum theoretical background, requirements, contents, marketed preparations, related questions, references and assessment scheme. The manual has been designed with more emphasis on the practical skill improvement of the students so that the students can perform the practical with ease and comfort. Hope this manual will help the students to learn the concept, principles and perform the experiments virtually. We wish you all the best!!!
Download or read book The Ayurvedic Pharmacopoeia of India written by and published by . This book was released on 2001 with total page 502 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Unani Pharmacopoeia of India written by and published by . This book was released on 2008 with total page 266 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Indian Pharmacopoeia 2014 4 Vol Set written by Indian Pharmacopoeia Commission and published by . This book was released on 2013-11-01 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: The seventh edition of the Indian Pharmacopoeia (IP 2014) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Government of India, Ministry of Health & Family Welfare. The Indian Pharmacopoeia (IP) is published in fulfilment of the requirements of the Drugs and Cosmetics Act, 1940 and Rules thereunder. It prescribes the standards for drugs produced and/or marketed in India and thus contributes in the control and assurance of the quality of the medicines. The standards of this pharmacopoeia are authoritative and legally enforceable. It intends to help in the licensing of manufacturing, inspection and distribution of medicines. IP is published in continuing pursuit of the mission of IPC to improve the health of the people through ensuring the quality, safety and efficacy of medicines. The Commission has been receiving significant inputs from regulatory, industrial houses, academic institutions, national laboratories, individual scientists and others. Publication of IP at regular and shorter intervals is one of the main mandates of the Commission. The seventh edition of Indian Pharmacopoeia is published in accordance with the principles and designed plan decided by the Scientific Body of the IPC. To establish transparency in setting standards for this edition the contents of new monographs, revised appendices and other informations have been publicized on the website of the IPC, besides following conventional approach of obtaining comments. The feedback and inputs were reviewed by the relevant Expert Committee to ensure the feasibility and practicability of the standards and methods revised. The principle of "openness, justice and fairness" is kept in mind during compiling and editing the contents of this edition. The Indian Pharmacopoeia 2014 is presented in four volumes. The scope of the Pharmacopoeia has been extended to include products of biotechnology, indigenous herbs and herbal products, veterinary vaccines
Download or read book Bentley s Textbook of Pharmaceutics E Book written by Sanjay Kumar Jain and published by Elsevier Health Sciences. This book was released on 2012-05-14 with total page 776 pages. Available in PDF, EPUB and Kindle. Book excerpt: This adaptation of Bentley's Textbook of Pharmaceutics follows the same goals as those of the previous edition, albeit in a new look. The content of the old edition has been updated and expanded and several new chapters, viz. Complexations, Stability Testing as per ICH Guidelines, Parenteral Formulations, New Drug Delivery Systems and Pilot Plant Manufacturing, have been included, with an intention to make the book more informative for the modern pharmacists. The book has six sections: Section I deals with the physicochemical principles. Two new chapters: Complexations and ICH Guidelines for Stability Testing, have been added to make it more informative. Section II conveys the information regarding pharmaceutical unit operations and processes. Section III describes the area of pharmaceutical practice. Extensive recent updates have been included in many chapters of this section. Two new chapters: Parenteral Formulations and New Drug Delivery Systems, have been added. Section IV contains radioactivity principles and applications. Section V deals with microbiology and animal products. Section VI contains the formulation and packaging aspects of pharmaceuticals. Pilot Plant Manufacturing concepts are added as a new chapter, which may be beneficial to readers to understand the art of designing of a plant from the pilot plant model.
Download or read book Countering the Problem of Falsified and Substandard Drugs written by Institute of Medicine and published by National Academies Press. This book was released on 2013-06-20 with total page 377 pages. Available in PDF, EPUB and Kindle. Book excerpt: The adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.
Download or read book Martindale written by Sean C. Sweetman and published by . This book was released on 2006-01-01 with total page 3335 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is thirty-fifth edition of Martindale, which provides reliable, and evaluated information on drugs and medicines used throughout the world. It contains encyclopaedic facts about drugs and medicines, with: 5,500 drug monographs; 128,000 preparations; 40,700 reference citations; 10,900 manufacturers. There are synopses of disease treatments which enables identification of medicines, the local equivalent and the manufacturer. It also Includes herbals, diagnostic agents, radiopharmaceuticals, pharmaceutical excipients, toxins, and poisons as well as drugs and medicines. Based on published information and extensively referenced
Download or read book The International Pharmacopoeia written by World Health Organization and published by World Health Organization. This book was released on 2006 with total page 1526 pages. Available in PDF, EPUB and Kindle. Book excerpt: The International Pharmacopoeia contains a collection of recommended methods for analysis and quality specifications for pharmaceutical substances, excipients and products. This new edition consolidates the texts of the five separate volumes of the third edition and includes new monographs for antiretroviral substances (didanosine, indinavir sulfate, nelfinavir mesilate, nevirapine, ritonavir, saquinovir, and saquinovir mesilate) adopted by the WHO Expert Committee on Specifications for Pharmaceutical Preparations in October 2004. It includes some additions and amendments to the general notices of the Pharmacopoeia, as well as some changes to its layout and format. Volume one contains monographs for pharmaceutical substances A to O and the General Notices; and volume two contains monographs for pharmaceutical substances P to Z, together with those for dosage forms and radiopharmaceutical preparations, the methods of analysis and reagents.
Download or read book A Text Book of Pharmaceutics 1 written by Prachi Pandey and published by JEC PUBLICATION. This book was released on with total page 213 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book having entitles “A Text Book of Pharmaceutics-I” (As Per Pharmacy Council of India, PCI Regulations). This text book is designed to impart a fundamental and theoretical knowledge on the art and sciences of various pharmaceutical dosage forms used in pharmaceutical industry as well as marketed level. This Pharmaceutics subjects deals with the various physical and physicochemical properties and their formulations/evaluations. The practice of the subject helps the students to get a better insight into the various areas of formulations research, development and stability studies of pharmaceutical dosage forms. The main objectives of the completion of this course students shall be able to: 01. Known the complete history of pharmacy profession since lastly. 02. Understand the basics of different dosage forms, pharmaceutical incompatibilities and pharmaceutical calculation involving in it. 03. Understand the professional ways to handling the prescriptions. This text book consists the various chapter in the form of units such as: Historical background and development of profession of pharmacy, Dosage forms, prescriptions, posology, pharmaceutical calculations, powders, liquid dosage forms, monophasic and Biphasic liquids, emulsions, suspensions, suppositories, pharmaceutical incompatibilities and semi-solid dosage forms. This book is designed according to the pharmacy council of India (PCI) curriculum of undergraduate courses in pharmacy specially for B. Pharm students, which mainly useful all over India. We sincerely request reader to send their valuable suggestions and constructive comments for making improvement in the text edition of the book. We extend out good wishes to the students and professor and sincerely hope to have the continued support from them and to our other books in future.
Download or read book WHO Monographs on Selected Medicinal Plants written by World Health Organization and published by World Health Organization. This book was released on 1999 with total page 392 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is the second volume in a series of monographs which are intended to promote information exchange and international harmonised standards for the quality control and use of herbal medicines. It contains scientific information on 30 selected plants, and each entry includes a pharmacopoeial summary for quality assurance purposes, information on its clinical application and sections on contraindications, pharmacology, safety issues, and dosage forms. It provides two cumulative indexes with entries in alphabetical order by plant name and according to the plant material of interest.
Download or read book Pharmacognosy written by Mr. S. B. Gokhale and published by Pragati Books Pvt. Ltd.. This book was released on 2008-08-07 with total page 334 pages. Available in PDF, EPUB and Kindle. Book excerpt:
