Wyniki wyszukiwania:
wyszukanych pozycji: 41
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
ISBN: 9781032917252 / Multiple-item retail product / 2024 / 2200 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
2688,26 |
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Biopharmaceutical Manufacturing, Volume 2: Unit processes
ISBN: 9780750331777 / Angielski / Twarda / 2022 / 350 str. Termin realizacji zamówienia: ok. 30 dni roboczych. |
cena:
617,40 |
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Biopharmaceutical Manufacturing, Volume 1: Regulatory processes
ISBN: 9780750331739 / Angielski / Twarda / 2021 / 350 str. Termin realizacji zamówienia: ok. 30 dni roboczych. |
cena:
617,40 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products
ISBN: 9781032918372 / Angielski Termin realizacji zamówienia: ok. 30 dni roboczych. |
cena:
236,62 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products
ISBN: 9781138103306 / Angielski / Twarda / 2019 / 502 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
1124,18 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile Products
ISBN: 9781032919737 / Angielski Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
224,78 |
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Filing Patents Online
ISBN: 9781138423060 / Angielski / Twarda / 2020 / 464 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
879,80 |
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Handbook of Bioequivalence Testing
ISBN: 9781482226379 / Angielski / Twarda / 2014 / 1007 str. Termin realizacji zamówienia: ok. 22 dni roboczych. As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence. In addition, advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more complex. The second edition of Handbook of Bioequivalence Testing has been completely updated to include the most current information available, including new findings in drug delivery and dosage form design... As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In rec... |
cena:
928,67 |
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The Future of Pharmaceuticals: A Nonlinear Analysis
ISBN: 9780367701390 / Angielski / Miękka / 2022 / 568 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
562,10 |
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Biosimilars and Interchangeable Biologics: Strategic Elements
ISBN: 9781138775503 / Angielski / Miękka / 2017 / 646 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
513,22 |
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Mrna Therapeutics: Fast-To-Market Strategies
ISBN: 9781032163444 / Angielski / Twarda / 2022 / 304 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
659,85 |
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Handbook of Preformulation: Chemical, Biological, and Botanical Drugs, Second Edition
ISBN: 9781138297555 / Angielski / Twarda / 2019 / 544 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
1075,31 |
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Handbook of Bioequivalence Testing
ISBN: 9781032917351 / Angielski Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
224,78 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Three, Liquid Products
ISBN: 9781138103221 / Angielski / Twarda / 2019 / 420 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
1124,18 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Five, Over-The-Counter Products
ISBN: 9781032919720 / Angielski Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
224,78 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile Products
ISBN: 9781138103832 / Angielski / Twarda / 2019 / 452 str. Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
1124,18 |
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Disposable Bioprocessing Systems
ISBN: 9781439866702 / Angielski / Twarda / 2012 / 322 str. Termin realizacji zamówienia: ok. 22 dni roboczych. Disposable systems are close to reaching the stage of development where they can replace current drug manufacturing methods. This book describes in detail the state-of-the-art systems used or under development for the manufacturing of biological drugs using disposable systems.
Disposable systems are close to reaching the stage of development where they can replace current drug manufacturing methods. This book describes in de...
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cena:
1001,99 |
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Three, Liquid Products
ISBN: 9781032920184 / Angielski Termin realizacji zamówienia: ok. 22 dni roboczych. |
cena:
224,78 |
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Biosimilars and Interchangeable Biologics: Tactical Elements
ISBN: 9781498743495 / Angielski / Twarda / 2015 / 575 str. Termin realizacji zamówienia: ok. 22 dni roboczych. What s the Deal with Biosimilars? Biosimilars are gaining momentum as new protein therapeutic candidates that can help fill a vital need in the healthcare industry. The biological drugs are produced by recombinant DNA technology that allows for large-scale production and an overall reduction time in costs and development. Part of a two-volume set that covers varying aspects of biosimilars, Biosimilars and Interchangeable Biologics: Tactical Elements explores the development and manufacturing of biosimilars and targets challenges surrounding the creation of these products. This... What s the Deal with Biosimilars? Biosimilars are gaining momentum as new protein therapeutic candidates that can help fill a vital need in the ... |
cena:
904,24 |
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Biosimilarity: The FDA Perspective
ISBN: 9781498750394 / Angielski / Twarda / 2018 / 436 str. Termin realizacji zamówienia: ok. 22 dni roboczych. The focus of this book is on how the US FDA will approve biosimilar drugs. The European scene is well developed with specific guidelines that are already in place. However, these guidelines do not apply to the thinking of the FDA in approving these products. The FDA is quite different from other regulatory agencies. With the US providing more than 50% of the worldwide market for these products, every serious manufacturer of biosimilar biological drugs should be targeting US approval of their products. Thus, this book is strictly on FDA approval strategy. The focus of this book is on how the US FDA will approve biosimilar drugs. The European scene is well developed with specific guidelines that are a... |
cena:
904,24 |
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