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Books on the topic 'Solid dosage form'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Carstensen, Jens Thurø. Pharmaceutical principles of solid dosage forms. Technomic Pub., 1993.

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2

Burrows, Jane L. Solid dosage forms for ophthalmic drug delivery. University of Portsmouth, 2002.

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3

1941-, Shargel Leon, and Kanfer Isadore, eds. Generic drug product development: Solid oral dosage forms. Marcel Dekker, 2005.

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4

Qiu, Yihong, Yisheng Chen, and Geoff G. Z. Zhang. Developing solid oral dosage forms: Pharmaceutical theory and practice. Edited by ScienceDirect (Online service). Academic, 2009.

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5

United States. Food and Drug Administration., ed. Bioequivalence of solid oral dosage forms: A presentation to the U.S. Food and Drug Administration hearing on bioequivalence of solid oral dosage forms September 29 - October 1, 1986. The Association, 1986.

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6

United States. Food and Drug Administration. Division of Field Investigations., ed. Guide to inspections of oral solid dosage forms pre/post approval issues for development and validation. Division of Field Investigations, Office of Regional Operations, Office of Regulatory Affairs, U.S. Food & Drug Administration, 1994.

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7

Storey, Richard A., and Ingvar Ymen. Solid state characterization of pharmaceuticals. John Wiley & Sons, 2011.

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8

J, Habib Muhammad, ed. Pharmaceutical solid dispersion technology. Technomic Pub. Co., 2001.

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9

United States. Food and Drug Administration. Division of Field Investigations, ed. Guide to inspections of oral solid dosage forms pre/post approval issues for development and validation. Division of Field Investigations, Office of Regional Operations, Office of Regulatory Affairs, U.S. Food & Drug Administration, 1994.

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10

G, Brittain H., ed. Polymorphism of pharmaceutical solids. 2nd ed. Informa Healthcare, 2009.

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11

G, Brittain H., ed. Physical characterization of pharmaceutical solids. M. Dekker, 1995.

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12

G, Brittain H., ed. Spectroscopy of pharmaceutical solids. Taylor & Francis, 2006.

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13

G, Brittain H., ed. Polymorphism in pharmaceutical solids. M. Dekker, 1999.

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14

Shargel, Leon. Generic drug product development. CRC, 2007.

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15

Isadore, Kanfer, and Shargel Leon 1941-, eds. Generic drug product development: Bioequivalence issues. Informa Healthcare, 2008.

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16

Preformulation solid dosage form development. Informa Healthcare USA, 2008.

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17

Adeyeye, Moji Christianah, and Harry G. Brittain, eds. Preformulation in Solid Dosage Form Development. CRC Press, 2008. http://dx.doi.org/10.3109/9780849360862.

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18

Brittain, Harry G., and Moji Christianah Adeyeye. Preformulation in Solid Dosage Form Development. Taylor & Francis Group, 2008.

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19

Brittain, Harry G., and Moji Christianah Adeyeye. Preformulation in Solid Dosage Form Development. Taylor & Francis Group, 2008.

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20

Akhter, Sharmin, M. Mohi Uddin Chowdhury, and Mohammed Ibrahim. Preparation of Herbal Solid Dosage Form. GRIN Verlag GmbH, 2017.

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21

(Editor), Moji C. Adeyeye, and Harry G. Brittain (Editor), eds. Preformulation in Solid Dosage Form Development (Drugs and the Pharmaceutical Sciences). Informa Healthcare, 2008.

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22

Al-Rifai, Noor. Pharmaceutical Engineering : a Primer for Advanced Process Development : Volume 2: Solid Dosage Form Process Design. Elsevier, 2024.

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23

Al-Rifai, Noor. Pharmaceutical Engineering : a Primer for Advanced Process Development. Volume 2: Solid Dosage Form Process Design. Elsevier, 2024.

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24

Marche, Keirnan La, and Eric Jayjock. Continuous Manufacturing in the Pharmaceutical Industry: Design, Control, and Implementation for Solid Dosage Form Production. Wiley & Sons, Incorporated, John, 2023.

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25

Marche, Keirnan La. Continuous Manufacturing in the Pharmaceutical Industry: Design, Control, and Implementation for Solid Dosage Form Production. Wiley & Sons, Limited, John, 2015.

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26

Edwards, Rodger. Solid Dosage Forms. Butterworth-Heinemann Medical, 2005.

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27

Developing Solid Oral Dosage Forms. Elsevier, 2009. http://dx.doi.org/10.1016/b978-0-444-53242-8.x0001-x.

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28

Carstensen, Jens T. Pharmaceutical Principles of Solid Dosage Forms. Taylor & Francis Group, 2014.

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29

Generic Drug Product Development: Solid Oral Dosage Forms. Taylor & Francis Group, 2013.

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30

Shargel, Leon, and Isadore Kanfer. Generic Drug Product Development: Solid Oral Dosage Forms. Taylor & Francis Group, 2014.

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31

Yu, Lawrence, Yihong Qiu, Yisheng Chen, Geoff G. Z. Zhang, and Rao V. Mantri. Developing Solid Oral Dosage Forms: Pharmaceutical Theory and Practice. Elsevier Science & Technology Books, 2016.

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32

Yu, Lawrence, Yihong Qiu, Yisheng Chen, Geoff G. Z. Zhang, and Rao V. Mantri. Developing Solid Oral Dosage Forms: Pharmaceutical Theory and Practice. Elsevier Science & Technology Books, 2016.

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33

Spireas, Spiro. Bioavailable/Bioequivalent Solid Dosage Forms of Water Insoluble Agents. CRC Press LLC, 1999.

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34

Ciper, Mesut. Fast disintegrating solid dosage forms for the Oral Cavity. 2004.

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35

Shargel, Leon, and Isadore Kanfer. Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition. Taylor & Francis Group, 2013.

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36

Shargel, Leon. Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition. Taylor & Francis Group, 2013.

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37

Shargel, Leon, and Isadore Kanfer. Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition. Taylor & Francis Group, 2013.

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38

Mittal, Bhavishya. How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval. Elsevier Science & Technology, 2016.

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39

Mittal, Bhavishya. How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval. Elsevier Science & Technology Books, 2016.

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40

Ispe. ISPE Baseline® Guide : Volume 2 - Oral Solid Dosage Forms: Chinese Translation. International Society for Pharmaceutical Engineering, 2011.

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41

Shargel, Leon. Generic Drug Development: Solid Oral Dosage Forms (Drugs and the Pharmaceutical Sciences). Informa Healthcare, 2004.

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42

Ispe. ISPE Baseline® Guide : Volume 2 - Oral Solid Dosage Forms: Japanese Translation. International Society for Pharmaceutical Engineering, 2011.

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43

Shargel, Leon, and Isadore Kanfer. Generic Drug Product Development: Specialty Dosage Forms. Taylor & Francis Group, 2016.

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44

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products. Taylor & Francis Group, 2019.

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45

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products. Taylor & Francis Group, 2019.

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46

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products. Taylor & Francis Group, 2019.

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47

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products. Taylor & Francis Group, 2019.

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48

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products. Taylor & Francis Group, 2019.

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49

Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products. Taylor & Francis Group, 2019.

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50

How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval. Elsevier, 2017. http://dx.doi.org/10.1016/c2015-0-01916-5.

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