2011 USP 34 ; NF 29 PDF Download
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Author: United States Pharmacopeial Convention
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 422
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Book Description
Author: United States Pharmacopeial Convention
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 422
Get Book Here
Book Description
Author:
Publisher:
ISBN: 9781889788920
Category :
Languages : en
Pages : 1713
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Book Description
Author: Usp
Publisher:
ISBN: 9781889788920
Category : Medical
Languages : en
Pages : 4638
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Book Description
Author: United States Pharmacopeial Convention
Publisher:
ISBN: 9781889788883
Category :
Languages : en
Pages : 668
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Book Description
Author: Antoine Al-Achi
Publisher: John Wiley & Sons
ISBN: 0470596929
Category : Medical
Languages : en
Pages : 1024
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Book Description
Focusing on the application of physical pharmacy, drug design, and drug regulations as they relate to produce effective dosage forms for drug delivery, Integrated Pharmaceutics provides a comprehensive picture of pharmaceutical product design, describing the science and art behind the concepts of dosage form development. Combining physical pharmacy, product design, and regulatory affairs issues in a single book, the authors address topics governing drug regulations of United States, European, and Japanese agencies and detail new regulatory guidelines, including quality by design, design space analysis, and blend sample uniformity.
Author: United States Pharmacopeial Convention
Publisher:
ISBN:
Category :
Languages : en
Pages : 1396
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Book Description
Author: Sanjay Kumar Jain
Publisher: Elsevier Health Sciences
ISBN: 8131232662
Category : Medical
Languages : en
Pages : 778
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Book Description
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.
Author: Anurag S. Rathore
Publisher: CRC Press
ISBN: 1439850941
Category : Medical
Languages : en
Pages : 532
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Book Description
Process Validation in Manufacturing of Biopharmaceuticals, Third Edition delves into the key aspects and current practices of process validation. It includes discussion on the final version of the FDA 2011 Guidance for Industry on Process Validation Principles and Practices, commonly referred to as the Process Validation Guidance or PVG, issued in
Author:
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 394
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Book Description
Author: Ali Nokhodchi
Publisher: John Wiley & Sons
ISBN: 1118799526
Category : Science
Languages : en
Pages : 392
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Book Description
Drug therapy via inhalation route is at the cutting edge of modern drug delivery research. There has been significant progress on the understanding of drug therapy via inhalation products. However, there are still problems associated with their formulation design, including the interaction between the active pharmaceutical ingredient(s) (APIs), excipients and devices. This book seeks to cover some of the most pertinent issues and challenges of such formulation design associated with industrial production and desirable clinical outcome. The chapter topics have been selected with a view to integrating the factors that require consideration in the selection and design of device and formulation components which impact upon patient usability and clinical effectiveness. The challenges involved with the delivery of macromolecules by inhalation to both adult and pediatric patients are also covered. Written by leading international experts from both academia and industry, the book will help readers (formulation design scientists, researchers and post-graduate and specialized undergraduate students) develop a deep understanding of key aspects of inhalation formulations as well as detail ongoing challenges and advances associated with their development.
