الصفحة 1
الصفحة 1
U.S. Pharmacopeia National Formulary 2018 USP 41 NF 36
Contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. Offers convenient, comprehensive information for all phases of producing quality prescription, nonprescription, and compounded medicines; excipients; biologics; medical devices; and dietary supplements. It is essential for quality control, quality assurance, regulatory/compendial affairs, research and development, method development/analytical services, and corporate management. USP–NF monographs and methods can help to: Ensure compliance with required U.S. quality standards / Work to world-recognized standards of precision and accuracy / Validate test results against proven benchmarks / Establish and validate in-house standard operating procedures, and specifications / Expedite new product development and approvals
Smart micro- and nanomaterials for drug delivery
Smart drug delivery at both the micro- and nanoscale is an evolving field with numerous potential applications. It has the potential to revolutionize drug therapy by making treatments more effective, reducing side effects, and improving patient outcomes. This book presents a comprehensive review of the most recent studies on smart micro- and nanomaterials with a focus on their “smart” activity for formation of targeted and responsive drug-delivery carriers.
Smart micro - and nanomaterials for pharmaceutical applications
Smart drug delivery refers to a targeted drug delivery or precision drug delivery system that allows drugs to be administered to a specific location in the body or at a specific time with enhanced precision and control. This approach has several advantages, including maximizing the therapeutic effects of a drug while minimizing side effects.
Polyvinylpyrrolidone Excipients for Pharmaceuticals : Povidone, Crospovidone and Copovidone
The book describes the properties, analytical methods and the applications of different polyvinylpyrrolidone excipients (povidone, crospovidone, copovidone etc.) for use in pharmaceutical preparations. This group of excipients is one of the most important excipients used in modern technology to produce drugs. The book is intended for all persons working in the research, development and quality control of drugs. It gives a survey of all applications in solid, liquid and semisolid dosage forms including many drug formulation examples and more than 600 references to the literature.
Pharmacy calculations : An introduction for pharmacy technicians ; 2nd ed.
Designed for pharmacy technician students enrolled in an education and training program, for technicians reviewing for the national certification exam, and for on-site training and professional development in the workplace. It provides a complete review of the basic mathematics concepts and skills upon which a more advanced understanding of pharmacy-related topics must be built
Pharmaceutical Powder and Particles
Reviews important aspects of powder and particle systems and the critical quality attributes that should be used as a guide to future developments intended to maximize the control of product quality and performance. Drs. Hickey and Giovagnoli have written an essential primer for any scientists involved in powder or particle research and manufacturing. Pharmaceutical Powder and Particles is appropriate for those just entering the field or as a rapid reference for the experienced pharmaceutical scientist.The authors have both academic and industrial experience and the coverage includes solid state chemistry; crystallization; physical processes; particle size and distribution; particle interaction; manufacturing processes; quality by design;and a general discussion of the industry.
Pharmaceutical formulation : The science and technology of dosage forms
Pharmaceutical Formulation provides an up to date source of information for all who wish to understand the principles and practice of formulation in the drug industry
Pharmaceutical facility design based on International approved GMP regulations
Pharmaceutical facility design is a project carried by contributors from different scientific backgrounds’; like pharmacists, engineers, pharmaceutical machine suppliers and regulatory organizations such as Current Good Manufacturing Practices (cGMP), World Health Organization (WHO), International Standardization Organization (ISO), United States Pharmacopeia (USP), and many other ones. And by that nature, the project needs to be tackled form various approaches pharmaceutical approach, architectural engineering approach, and regulatory approach. This study will illuminate on the requirements in terms of regulations, design features, and equipment for a facility intended for manufacturing solid and liquid dosage forms of drugs under the regulations of Current Good Manufacturing Practices (cGMP).
Pharmaceutical drug product development and process optimization : Effective Use of quality by design
Presents and discusses the vital precepts underlying the efficient, effective, and cost-effective development of pharmaceutical drug products. It focuses on the adoption of systematic quality principles of pharmaceutical development, which is imperative in achieving continuous improvement in end-product quality and also leads to reducing cost, time, and effort, while meeting regulatory requirements. Key features: Reviews a vast collection of literature on applicability of systematic product development tools / Discusses various dosage forms where challenges are very high / Provides regulatory guidance related specific dosage form development / Covers the major types of drug products, including enteral, parenteral, and other (including transdermal, inhalation, etc.)
Pharmaceutical dosage forms and drug delivery : Revised and expanded
Completely revised and updated, this fourth edition elucidates the principles of pharmaceutics, biopharmaceutics, dosage form design, and drug delivery - including emerging new biotechnology-based treatment modalities. The authors integrate aspects of physical pharmacy, chemistry, biology, and biopharmaceutics into drug delivery
Pharmaceutical Dosage Forms
The following project aims to definition of pharmaceutical dosage forms in general and talking about each dosage form separately the need of this dosage form, the methods used to manufacture this form and most used excipients and most important examples of APIs used in this form.
Pharmaceutical calculations : A conceptual approach
Combines conceptual and procedural understanding for students and will guide you to master prerequisite skills to carry out accurate compounding and dosage regimen calculations. It is a book that makes the connection between basic sciences and pharmacy. It describes the most important concepts in pharmaceutical sciences thoroughly, accurately and consistently through various commentaries and activities to make you a scientific thinker, and to help you succeed in college and licensure exams. Calculation of the error associated with a dose measurement can only be carried out after understanding the concept of accuracy versus precision in a measurement. Similarly, full appreciation of drug absorption and distribution to tissues can only come about after understanding the process of transmembrane passive diffusion.
Pharmaceutical biotechnology : fundamentals and applications
This introductory text explains both the basic science, production, quality, dosage forms, administration, economic and regulatory aspects and the clinical applications of biotechnology-derived pharmaceuticals. It serves as a complete one-stop source for undergraduate/graduate pharmacists and pharmaceutical science students. An additional important audience are pharmaceutical scientists in industry and academia, particularly those who have not received formal training in pharmaceutical biotechnology and are inexperienced in this field. The rapid growth and advances in the field made it necessary to revise this textbook in order to continue providing up-to-date information and introduce readers to cutting edge knowledge and technology of this field.
Modern pharmaceutics
Covers the curriculum and syllabus developed by the Pharmacy Council of India, providing students with the necessary knowledge and skills required in the field of pharmaceutical services
Modern aspects of pharmaceutical quality assurance : developing and proposing application models, SOPs, practical audit systems for pharma industry
Aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.
Integrated pharmaceutics : Applied preformulation, product design, and regulatory science
Provides a comprehensive introduction to the creation and manufacture of effective dosage forms for drug delivery. It presents its subject following the principles of physical pharmacy, product design, and drug regulations. This tripartite structure allows readers to move from theory to practice, beginning from a firm foundation ...
Innovative dosage forms : Design and development at early stage
Provides information that is essential for the drug development effort Presents the latest advances in the field and describes in detail innovative formulations, such as nanosuspensions, micelles, and cocrystals Describes current approaches in early pre-formulation to achieve the best in vivo results Addresses regulatory and safety aspects, which are key considerations for pharmaceutical companies Includes case studies from recent drug development programs to illustrate the practical challenges of preformulation design
In Vitro Drug Release Testing of Special Dosage Forms
Covers the in vitro release testing of: lipid based oral formulations; chewable oral drug products; injectables; drug eluting stents; inhalation products; transdermal formulations; topical formulations; vaginal and rectal delivery systems and ophthalmics. The book concludes with a look at regulatory aspects. Covers both oral and non-oral dosage forms Describes current regulatory conditions for in vitro drug release testing Features contributions from well respected global experts in dissolution testing
Hyaluronic Acid
Hyaluronic acid, also known as hyaluronan, is a clear, gooey substance that is naturally produced by your body, Hyaluronic acid is generally very safe to use, with few reported side effects. The largest amounts of it are found in your skin, connective tissue and eyes, and Hyaluronic acid has a variety of uses. Many people take it as a supplement, but it’s also used in topical serums, eye drops and injections, and the almost indications are Promotes Healthier, More Supple Skin, accelerate wound healing, Relieve Joint Pain by Keeping Bones Well Lubricated, reduce symptoms of acid reflux, Relieve Dry Eye and Discomfort, Preserve Bone Strength and Prevent Bladder Pain.
Handbook of pharmaceutical manufacturing formulations ; Vol.6 : Sterile products
An authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this six-volume set compiles data from FDA new drug applications, patent applications, and other sources of generic and proprietary formulations to cover the broad spectrum of GMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent
