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wyszukanych pozycji: 7
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Bioequivalence Requirements in Various Global Jurisdictions
ISBN: 9783319680774 / Angielski / Twarda / 2017 / 345 str. Termin realizacji zamówienia: ok. 20 dni roboczych. |
cena:
854,08 zł |
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Bioequivalence Requirements in Various Global Jurisdictions
ISBN: 9783319885421 / Angielski / Miękka / 2018 / 345 str. Termin realizacji zamówienia: ok. 20 dni roboczych. |
cena:
854,08 zł |
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Generic Drug Product Development: Bioequivalence Issues
ISBN: 9780849377846 / Angielski / Twarda / 2007 / 288 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be interchangeable. The demonstration of bioequivalence is an important component of therapeutic equivalence. Bioequivalence studies are very expensive, time consuming and always have the possibility of failure. The objective of this textbook is to describe some of those specific bioequivalence issues which need to be...
The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counter...
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cena:
885,18 zł |
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Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
ISBN: 9780849377853 / Angielski / Twarda / 2010 / 332 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutically equivalent to the brand name alternative. However, many countries have limited resources to inspect and verify the quality of all drug products for sale in their country. This title discusses the worldwide legislative and regulatory requirements...
Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent ...
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cena:
885,18 zł |
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Generic Drug Product Development: Specialty Dosage Forms
ISBN: 9780367384395 / Angielski / Miękka / 2019 / 288 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
322,78 zł |
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Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
ISBN: 9780367384371 / Angielski / Miękka / 2019 / 332 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
322,78 zł |
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Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition
ISBN: 9781032920603 / Angielski Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
239,46 zł |
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