Lawrence x yu (29 risultati)
Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Hardcover. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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Lingua: Inglese
Editore: Springer New York, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: moluna, Greven, Germaniamoluna
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Gebunden. Condizione: New.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Ria Christie Collections, Uxbridge, Regno UnitoRia Christie Collections
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Condizione: New. In.
Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Ria Christie Collections, Uxbridge, Regno UnitoRia Christie Collections
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Lingua: Inglese
Editore: Springer New York, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Condizione: New.
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Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Taschenbuch. Condizione: Neu. FDA Bioequivalence Standards | Lawrence X. Yu (u. a.) | Taschenbuch | AAPS Advances in the Pharmaceutical Sciences Series | xiii | Englisch | 2016 | Springer | EAN 9781493955589 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]sp…ringer[dot]com | Anbieter: preigu.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Books Puddle, New York, NY, U.S.A.Books Puddle
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Condizione: New. pp. 465.
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Lingua: Inglese
Editore: Springer New York, Springer US, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its origin and principles, sta…tistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards.
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Lingua: Inglese
Editore: Springer, Humana, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its origin and principl…es, statistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards.
Lingua: Inglese
Editore: SPRINGER, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Edizione Internazionale
Da: UK BOOKS STORE, London, LONDO, Regno UnitoUK BOOKS STORE
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Condizione: New Books. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requeste…d if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.
Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Revaluation Books, Exeter, Regno UnitoRevaluation Books
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Hardcover. Condizione: Brand New. 1st edition. 465 pages. 9.25x6.25x1.50 inches. In Stock.
Lingua: Inglese
Editore: Springer Verlag, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Revaluation Books, Exeter, Regno UnitoRevaluation Books
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Paperback. Condizione: Brand New. reprint edition. 478 pages. 9.25x6.10x1.13 inches. In Stock.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Mispah books, Redhill, SURRE, Regno UnitoMispah books
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Paperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
Lingua: Inglese
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Da: liu xing, Nanjing, JS, Cinaliu xing
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paperback. Condizione: New. Paperback. Pub Date: 2022-06-01 Pages: 821 Language: Chinese Publisher: Renmin University Press Helping Skills: Individual. Family. Group. and Community Work Methods (Eighth Edition) shows how social workers differ from Common elements. core processes. and skills that exist at all stages of working to…gether and providing services to individuals. such as individuals. families. groups. or community organizations. The book expounds a wide range of helping situations. clearly defines. illustrates.
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Clinical treatment of diabetes (translation)(Chinese Edition)
[ MEI ] David G.Armstrong . Lawrence A.Lavery BIAN . DENG WU QUAN . XU ZHANG RONG . MA YU YI
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Da: liu xing, Nanjing, JS, Cinaliu xing
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paperback. Condizione: New. Paperback. Pub Date: 100 language: Chinese Publisher: People's Health Publishing House This book is a guide to the diabetic foot treatment of American diabetes. divided into 12 chapters. which introduces the etiology. screening and evaluation of diabetic foot. Grading. decompression treatment. cleanin…g treatment. infection treatment. vascular assessment and multidisciplinary joint diabetes foot diagnosis.
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Da: liu xing, Nanjing, JS, Cinaliu xing
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paperback. Condizione: New. Language:Chinese.Paperback. Pub Date: 2022-11-01 Publisher: Shanghai Jiao Tong University Press This book reviews the origin and evolution of large commercial aircraft trade disputes. analyzes and estimates the U.S. governments investment in the upstream and downstream of the civil aircraft manufactur…ing industry chain from 1992 to 1998 The amount of subsidies implemented by the enterprise. Through in-depth analysis. this book explains the impact of changes in transatlantic relations on the t.
Editore: China Renmin University Press, 2022
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Da: liu xing, Nanjing, JS, Cinaliu xing
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EUR 199,78
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paperback. Condizione: New. Paperback. Pub Date: 2022-06-01 Pages: 821 Language: Chinese Publisher: Renmin University Press Helping Skills: Individual. Family. Group. and Community Work Methods (Eighth Edition) shows how social workers differ from Common elements. core processes. and skills that exist at all stages of working to…gether and providing services to individuals. such as individuals. families. groups. or community organizations. The book expounds a wide range of helping situations. clearly defines. illustrates.
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Da: liu xing, Nanjing, JS, Cinaliu xing
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Hardcover. Condizione: New. HardCover. Pub Date: 2017-01-01 Pages: 438 Language: Chinese Publisher: Beijing medical university press standard of FDA bioequivalence this comprehensive reference book shows the status quo of drug regulation of bioequivalence scientific practice and recent exhibition.The journal of the American asso…ciation of pharmaceutical scientists (AAPS) progress in pharmaceutical science books: the FDA creatures. etc.
Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Basi6 International, Irving, TX, U.S.A.Basi6 International
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Condizione: Brand New. New. US edition. Print on demand title. Delivery takes 20-25 days. Excellent Customer Service.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: Basi6 International, Irving, TX, U.S.A.Basi6 International
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Condizione: Brand New. New. US edition. Print on demand title. Delivery takes 20-25 days. Excellent Customer Service.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Brook Bookstore On Demand, Napoli, NA, ItaliaBrook Bookstore On Demand
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Condizione: new. Questo è un articolo print on demand.
Lingua: Inglese
Editore: Springer, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: Brook Bookstore On Demand, Napoli, NA, ItaliaBrook Bookstore On Demand
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Condizione: new. Questo è un articolo print on demand.
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Lingua: Inglese
Editore: Springer New York, Springer US Sep 2016, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its ori…gin and principles, statistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards. 480 pp. Englisch.
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Lingua: Inglese
Editore: Springer New York, Springer US Sep 2014, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Buch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its origin and… principles, statistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards. 480 pp. Englisch.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: Majestic Books, Hounslow, Regno UnitoMajestic Books
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Condizione: New. Print on Demand pp. 465.
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Lingua: Inglese
Editore: Springer New York, Springer US Sep 2014, 2014
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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- Print on Demand
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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EUR 246,09
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Buch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its origin and pri…nciples, statistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 480 pp. Englisch.
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Lingua: Inglese
Editore: Springer, Humana Sep 2016, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
- Brossura
- Print on Demand
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 246,09
EUR 60,00 spedizioneSpedito da Germania a U.S.A.Quantità: 1 disponibili
Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This comprehensive reference provides an in-depth discussion on state-of-the-art regulatory science in bioequivalence. In sixteen chapters, the volume explores a broad range of topics pertaining to bioequivalence, including its origin…and principles, statistical considerations, food effect studies, conditions for waivers of bioequivalence studies, Biopharmaceutics Classification Systems, Biopharmaceutics Drug Disposition Classification System, bioequivalence modeling/simulation and best practices in bioanalysis. It also discusses bioequivalence studies with pharmacodynamic and clinical endpoints as well as bioequivalence approaches for highly variable drugs, narrow therapeutic index drugs, liposomes, locally acting gastrointestinal drug products, topical products and nasal and inhalation products.FDA Bioequivalence Standards is written by FDA regulatory scientists who develop regulatory policies and conduct regulatory assessment of bioequivalence. As such, both practical case studies and fundamental science are highlighted in these chapters. The book is a valuable resource for scientists who work in the pharmaceutical industry, regulatory agencies and academia as well as undergraduate and graduate students looking to expand their knowledge about bioequivalence standards.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 480 pp. Englisch.
Lingua: Inglese
Editore: Springer, 2016
Serie: Libro 12 di 38 - AAPS Advances in the Pharmaceutical Sciences
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Da: Biblios, frankfurt am main, HESSE, GermaniaBiblios
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Condizione: New. PRINT ON DEMAND pp. 465.
