Drug Formulations Manual Third Edition D P S Kohli Amp D H Shah Downloads Torrent !FULL!
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Drug Formulations Manual: A Comprehensive Guide for Pharmaceutical Professionals
Drug Formulations Manual is a book that provides practical and up-to-date information on various aspects of drug formulation, manufacturing, quality control, and analysis. The book covers topics such as dosage forms, excipients, stability, bioavailability, dissolution, packaging, labeling, and regulatory requirements. The book also includes more than 500 formulations of various drugs for oral, topical, parenteral, ophthalmic, nasal, and rectal administration.
The book is written by D. P. S. Kohli and D. H. Shah, who are both experienced pharmaceutical professionals with over 40 years of combined experience in the industry. They have authored several books and articles on pharmaceutical sciences and have been involved in teaching and training programs for students and professionals.
The third edition of the book was published in 2008 by Eastern Publishers and contains 506 pages. The book is intended for students, teachers, researchers, pharmacists, formulators, quality assurance personnel, and regulatory affairs professionals who are interested in learning more about drug formulations and their development.
The book is available in print format only and can be purchased from various online and offline sources. However, some people may try to download the book illegally from torrent sites or other file-sharing platforms. This is not only unethical but also illegal and may expose the users to malware, viruses, or legal consequences.
Therefore, it is strongly recommended that anyone who wants to read the book should buy it from a legitimate source and respect the intellectual property rights of the authors and publishers.
Drug Formulations Manual is divided into 12 chapters that cover the following topics:
Chapter 1: Introduction to drug formulations and their importance in drug development and delivery.
Chapter 2: Principles and methods of drug formulation, including preformulation studies, selection of dosage forms and excipients, compatibility studies, and scale-up and optimization techniques.
Chapter 3: Oral solid dosage forms, such as tablets, capsules, powders, granules, and pellets. The chapter discusses the types, advantages, disadvantages, formulation factors, manufacturing processes, quality control tests, and stability studies of these dosage forms.
Chapter 4: Oral liquid dosage forms, such as solutions, suspensions, emulsions, syrups, elixirs, and drops. The chapter discusses the types, advantages, disadvantages, formulation factors, manufacturing processes, quality control tests, and stability studies of these dosage forms.
Chapter 5: Topical dosage forms, such as creams, ointments, gels, lotions, pastes, plasters, and patches. The chapter discusses the types, advantages, disadvantages, formulation factors, manufacturing processes, quality control tests, and stability studies of these dosage forms.
Chapter 6: Parenteral dosage forms, such as injections, infusions, implants, and depot preparations. The chapter discusses the types, advantages, disadvantages, formulation factors, manufacturing processes, quality control tests, and stability studies of these dosage forms.
Chapter 7: Ophthalmic dosage forms, such as eye drops, eye ointments, eye gels,
and eye inserts. The chapter discusses the types,
advantages,
disadvantages,
formulation factors,
manufacturing processes,
quality control tests,
and stability studies of these dosage forms.
Chapter 8: Nasal dosage forms,
such as nasal drops,
nasal sprays,
nasal gels,
and nasal powders. The chapter discusses the types,
advantages,
disadvantages,
formulation factors,
manufacturing processes,
quality control tests,
and stability studies of these dosage forms.
Chapter 9: Rectal and vaginal dosage forms,
such as suppositories,
pessaries,
enemas,
and douches. The chapter discusses the types,
advantages,
disadvantages,
formulation factors,
manufacturing processes,
quality control tests,
and stability studies of these dosage forms.
Chapter 10: Bioavailability and bioequivalence of drug formulations. The chapter explains the concepts,
factors affecting bioavailability and bioequivalence,
methods of assessment,
and regulatory requirements for bioavailability and bioequivalence studies.
Chapter 11: Dissolution testing of drug formulations. The chapter explains the importance,
principles,
methods,
apparatuses,
and specifications for dissolution testing of various dosage forms.
Chapter 12: Packaging and labeling of drug formulations. The chapter discusses the functions,
types,
materials,
designs,
and specifications for packaging and labeling of various dosage forms.
The book also contains several appendices that provide useful information on various topics related to drug formulations,such as pharmacopoeial standards,solubility data,stability data,pH adjustment,buffers,isotonicity,preservatives,colorants,and flavorants.
The book is written in a clear and concise manner with numerous examples,t
ables,and figures to illustrate the concepts and techniques. The book also provides references for further reading at the end of each chapter. aa16f39245