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Subjects
Drugs, Drug development, Testing, Law and legislation, Pharmaceutical industry, Pharmaceutical technology, Medical / Pharmacology, Pharmacology, Medical, Medical / Nursing, Generic drugs, Drugs, generic substitution, Drugs, dosage, Solid dosage forms, Generic Drugs, Standards, Pharmaceutical Chemistry, Drug Approval, Tablets, Dosage forms, Therapeutic equivalency, Dosage Forms, Biopharmaceutics, Methods, Therapeutic EquivalencyShowing 11 featured editions. View all 11 editions?
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01
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
2016, Taylor & Francis Group
in English
0429132913 9780429132919
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02
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
2016, Taylor & Francis Group
in English
1420020021 9781420020021
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03
Generic Drug Product Development: Specialty Dosage Forms
2016, Taylor & Francis Group
in English
142002003X 9781420020038
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04
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence, Second Edition
2016, Taylor & Francis Group
in English
1466599626 9781466599628
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05
Generic Drug Product Development: Solid Oral Dosage Forms
2013, Taylor & Francis Group, CRC Press/Taylor & Francis Group
in English
1420086359 9781420086355
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06
Generic Drug Product Development: Specialty Drug Products
December 15, 2010, Informa Healthcare
Hardcover
in English
- 1 edition
0849377862 9780849377860
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07
Generic drug product development: bioequivalence issues
2008, Informa Healthcare
in English
0849377846 9780849377846
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08
Generic Drug Product Development: Bioequivalence Issues
2007, Taylor & Francis Group
in English
1420020013 9781420020014
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09
Generic Drug Product Development: Bioequivalence Issues
2007, Taylor & Francis Group
in English
0429132905 9780429132902
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10 |
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11
Generic drug product development
2007, CRC, Taylor & Francis [distributor]
in English
0849377862 9780849377860
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- Created September 17, 2021
- 1 revision
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September 17, 2021 | Created by ImportBot | Imported from Better World Books record |