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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 EquivalencyEdition | Availability |
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01
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence, Second Edition
2016, Taylor & Francis Group
in English
1466599626 9781466599628
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02
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
2016, Taylor & Francis Group
in English
0429132913 9780429132919
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03
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
2016, Taylor & Francis Group
in English
1420020021 9781420020021
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04
Generic Drug Product Development: Specialty Dosage Forms
2016, Taylor & Francis Group
in English
142002003X 9781420020038
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aaaa
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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
2007, CRC, Taylor & Francis [distributor]
in English
0849377862 9780849377860
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10 |
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11
Generic Drug Product Development: Bioequivalence Issues
2007, Taylor & Francis Group
in English
0429132905 9780429132902
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zzzz
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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 |