Quality by Design approach for studying the impact of formulation and process variables on product quality of oral disintegrating films-Reference-Cited by-同舟云学术

Quality by Design approach for studying the impact of formulation and process variables on product quality of oral disintegrating films

Published:2017-07 Issue:1-2 Volume:527 Page:151-160
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Mazumder Sonal,Pavurala Naresh,Manda Prashanth,Xu Xiaoming,Cruz Celia N.,Krishnaiah Yellela S.R.

Funder

ORISE Research Participation Program at CDER administered by the Oak Ridge Institute for Science and Education

U.S. Department of Energy

CDER

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference35 articles.

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3. Oral films: current status and future perspectives: i – Galenical development and quality attributes;Borges;J. Control Release,2015

4. Using definitive screening design to effectively assess the combinatorial impacts of media supplements on monoclonal antibody production in mammalian cells;Chen,2016

5. Bioequivalence of ondansetron oral soluble film 8 mg (ZUPLENZ) and ondansetron orally disintegrating tablets 8 mg (ZOFRAN) in healthy adults;Dadey;Am. J. Ther.,2015

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