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.

Author/creator Mittal, Bhavishya
Format Electronic
Publication InfoAmsterdam ; Boston : Elsevier/Academic Press, [2017]
Descriptionxxii, 168 pages : illustrations, portrait ; 23 cm.
Supplemental ContentFull text available from eBook - Pharmacology, Toxicology and Pharmaceutical Science 2016 [EBCPTPS16]
Subjects
Pharmacology.
Drugs--Dosage forms.
Dosage Forms.
Administration, Oral.
Technology, Pharmaceutical.

SeriesExpertise in pharmaceutical process technology series
Expertise in pharmaceutical process technology series. UNAUTHORIZED
Abstract 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.
Bibliography noteIncludes bibliographical references and index.
Access restrictionAvailable only to authorized users.
Technical detailsMode of access: World Wide Web
Genre/formElectronic books.
LCCN 2016942143
ISBN9780128047316 (pbk)
ISBN0128047313 (pbk)

Availability

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Electronic Resources Access Content Online ✔ Available