How to develop robust solid oral dosage forms : from conception to post-approval / Bhavishya Mittal ; series editor, Michael Levin, Milev, LLC, Pharmaceutical Technology Consulting, West Orange, NJ, United States.

By:

Mittal, Bhavishya [author.]

Series: Expertise in pharmaceutical process technology seriesPublisher: Amsterdam ; London: Boston : Elsevier/Academic Press, [2017]Description: xxii, 168 pages : illustrations, portrait ; 23 cmContent type:

text

Media type:

unmediated

Carrier type:

volume

ISBN:

9780128047316 (pbk)
0128047313 (pbk)

Subject(s):

DDC classification:

615.1 23 M685

Summary: How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms.-- Source other than the Library of Congress.

Item type:

كتاب

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Holdings ( 1 )
Title notes ( 2 )

Holdings
Item type	Current library	Call number	Status	Notes	Date due	Barcode
كتاب	Central Library المكتبة المركزية	615.1 M685 (Browse shelf(Opens below))	Available	قاعة الكتب

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Previous	615.1 C596 Goth's medical pharmacology.	615.1 J54 Pharmacology and drug Administration for imaging technologists/	615.1 L 729 Pharmacology and the nursing process /	615.1 M685 How to develop robust solid oral dosage forms : from conception to post-approval /	615.1 O34 Calculation of drug dosages : a work text /	615.1 R137 Netter's illustrated pharmacology /	615.1 T943 Clinical pharmacology and practical prescribing on the move /	Next

Includes bibliographical references and index.

How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms.-- Source other than the Library of Congress.