LAB MANUAL OF PHARMACEUTICAL ENGINEERING PDF Download
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Author: Dr. Sonia Narwal, Ms. Preeti, Mrs. Prarthna Lakhera, Ms.Sneha Anand
Publisher: Shashwat Publication
ISBN: 8119281306
Category : Computers
Languages : en
Pages : 64
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Book Description
Pharmaceutical Engineering is a branch of Pharmaceutical technology that deals with the study of various principles involved in unit operations during dosage form manufacturing. A humble attempt was made to design the experiments in a concise, precise and systematic manner strictly as per the guidelines of Pharmacy Council of India to fulfill the need of Pharmacy teachers and students. This book contains well-defined experiments. Each experiment provides the theoretical background to the students. This practical book is designed in very simple and lucid language.
Author: Dr. Sonia Narwal, Ms. Preeti, Mrs. Prarthna Lakhera, Ms.Sneha Anand
Publisher: Shashwat Publication
ISBN: 8119281306
Category : Computers
Languages : en
Pages : 64
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Book Description
Pharmaceutical Engineering is a branch of Pharmaceutical technology that deals with the study of various principles involved in unit operations during dosage form manufacturing. A humble attempt was made to design the experiments in a concise, precise and systematic manner strictly as per the guidelines of Pharmacy Council of India to fulfill the need of Pharmacy teachers and students. This book contains well-defined experiments. Each experiment provides the theoretical background to the students. This practical book is designed in very simple and lucid language.
Author: Mrs. B. Jeevana Jyothi
Publisher: Nirali Prakashan
ISBN: 9788185790640
Category :
Languages : en
Pages : 68
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Book Description
Author: Ramesh Adepu
Publisher: Pharmamed Press
ISBN: 9789385433900
Category : Medical
Languages : en
Pages : 236
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Book Description
In India, Community Pharmacy Practice is considered as retail store pharmacy where the primary focus is trade. Although the concept of pharmacy practice is well defined and appreciated and practiced in western part of the world since 90's, in India, it is growing concept. Patient focused practice is slowly realizing with introduction of clinical pharmacy education in India since 1996. Unfortunately lack of trained staff, non availability of the text books to meet the academic needs of students studying pharmacy practice was a big challenge. To overcome this challenge, a sincere effort was made to bring out this text book on community pharmacy practice. The Text book covers Scope and Growth of Community Pharmacy Practice Pharmaceutical Care practices Pharmacy Management Patient focused Services Ethics in Pharmacy Practice
Author: Elsevier Inc
Publisher: Elsevier Health Sciences
ISBN: 0323765181
Category : Medical
Languages : en
Pages : 433
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Book Description
This easy-to-use, chapter-by-chapter companion to Mosby's Pharmacy Technician: Principles and Practice, 6th Edition helps you solidify your understanding and mastery of key skills and concepts. Each chapter of this combination workbook and lab manual contains a wide variety of review questions, exercises, and experiential lab activities to help reinforce key concepts, encourage you to reflect critically, and relate to practice for success on the job. Combined with the core textbook, this learning package takes you from day one through graduation and certification! - Comprehensive content aligns with ASHP competencies and certification exam coverage. - Reinforce Key Concepts sections offer valuable review and practice. - Reflect Critically sections with realistic scenarios encourage content assimilation and application. - Relate to Practice sections with laboratory exercises provide hands-on practice to promote multi-dimensional skills mastery. - Skills checklists correlated to textbook procedures enable you to track your progress on key competencies. - NEW! Additional content ensures thorough coverage of all entry-level and many advanced ASHP accreditation competencies, including: - Wellness, disease prevention, and immunizations - Medication compliance and point-of-care testing - Professional and regulatory standards - Medication requiring special handling and documentation - Nonsterile and sterile compounding - Advanced Pharmacy Technician duties
Author: Syed Imtiaz Haider
Publisher: CRC Press
ISBN: 143985016X
Category : Medical
Languages : en
Pages : 484
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Book Description
Written to help companies comply with GMP, GLP, and validation requirements imposed by the FDA and regulatory bodies worldwide, Quality Control Training Manual: Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories presents cost-effective training courses that cover how to apply advances in the life sciences
Author: Bryan Howard
Publisher: CRC Press
ISBN: 1439824932
Category : Medical
Languages : en
Pages : 439
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Book Description
COST (European Cooperation in the field of Scientific and Technical Research) is an intergovernmental initiative in science and research intended to promote the coordination of nationally funded research in Europe. Four working groups discuss the housing of animals, their environmental needs, refinement of procedures, genetically modified animals, and cost-benefit analysis. Based on the activities of these working groups, this book provides the European best practices for individuals and institutions working with laboratory animals. The text also discusses the ethical evaluation of experiments and procedures involving animals.
Author: EduGorilla Prep Experts
Publisher: EduGorilla Community Pvt. Ltd.
ISBN: 9358801948
Category :
Languages : en
Pages : 177
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Book Description
Author: Shayne Cox Gad
Publisher: John Wiley & Sons
ISBN: 0470259809
Category : Science
Languages : en
Pages : 1386
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Book Description
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Author: Mary T. am Ende
Publisher: John Wiley & Sons
ISBN: 1119285518
Category : Technology & Engineering
Languages : en
Pages : 686
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Book Description
A guide to the important chemical engineering concepts for the development of new drugs, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry offers a guide to the experimental and computational methods related to drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design and process development of drug products. The authors review basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, that are addressed with consideration of the applied statistics, process analytical technology, and process control. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API’s) and 2) Drug Product Design, Development and Modeling. The contributors explore technology transfer and scale-up of batch processes that are exemplified experimentally and computationally. Written for engineers working in the field, the book examines in-silico process modeling tools that streamline experimental screening approaches. In addition, the authors discuss the emerging field of continuous drug product manufacturing. This revised second edition: Contains 21 new or revised chapters, including chapters on quality by design, computational approaches for drug product modeling, process design with PAT and process control, engineering challenges and solutions Covers chemistry and engineering activities related to dosage form design, and process development, and scale-up Offers analytical methods and applied statistics that highlight drug product quality attributes as design features Presents updated and new example calculations and associated solutions Includes contributions from leading experts in the field Written for pharmaceutical engineers, chemical engineers, undergraduate and graduation students, and professionals in the field of pharmaceutical sciences and manufacturing, Chemical Engineering in the Pharmaceutical Industry, Second Edition contains information designed to be of use from the engineer's perspective and spans information from solid to semi-solid to lyophilized drug products.
Author: Kim Huynh-Ba
Publisher: John Wiley & Sons
ISBN: 1119120918
Category : Science
Languages : en
Pages : 420
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Book Description
Provides practical guidance on pharmaceutical analysis, written by leading experts with extensive industry experience Analytical Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while maintaining compliance with Good Manufacturing Practices (GMP) regulations. Concise yet comprehensive chapters contain up-to-date coverage of drug regulations, pharmaceutical analysis methodologies, control strategies, testing development and validation, method transfer, electronic data documentation, and more. Each chapter includes a table of contents, definitions of acronyms, a reference list, and ample tables and figures. Addressing the principal activities and regulatory challenges of analytical testing in the development and manufacturing of pharmaceutical drug products, this authoritative resource: Describes the structure, roles, core guidelines, and GMP regulations of the FDA and ICH. Covers the common analytical technologies used in pharmaceutical laboratories, including examples of analytical techniques used for the release and stability testing of drugs. Examines control strategies established from quality systems supported by real-world case studies. Explains the use of dissolution testing for products such as extended-release capsules, aerosols, and inhalers. Discusses good documentation and data reporting practices, stability programs, and the Laboratory Information Management System (LIMS) to maintain compliance. Includes calculations, application examples, and illustrations to assist readers in day-to-day laboratory operations. Contains practical information and templates to structure internal processes or common Standard Operating Procedures (SOPs). Analytical Testing for the Pharmaceutical GMP Laboratory is a must-have reference for both early-career and experienced pharmaceutical scientists, analytical chemists, pharmacists, and quality control professionals. It is also both a resource for GMP laboratory training programs and an excellent textbook for undergraduate and graduate courses of analytical chemistry in pharmaceutical sciences or regulatory compliance programs.
