Da: Basi6 International, Irving, TX, U.S.A.
Condizione: Brand New. New.SoftCover International edition. Different ISBN and Cover image but contents are same as US edition.Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
Da: ThriftBooks-Dallas, Dallas, TX, U.S.A.
Hardcover. Condizione: Very Good. No Jacket. May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less.
Da: PBShop.store US, Wood Dale, IL, U.S.A.
EUR 15,60
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Aggiungi al carrelloPAP. Condizione: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Da: PBShop.store UK, Fairford, GLOS, Regno Unito
EUR 13,85
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Aggiungi al carrelloPAP. Condizione: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Da: SHIMEDIA, Brooklyn, NY, U.S.A.
Condizione: New. Satisfaction Guaranteed or your money back.
Da: GreatBookPrices, Columbia, MD, U.S.A.
Condizione: As New. Unread book in perfect condition.
Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 243,63
Quantità: 9 disponibili
Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: GreatBookPrices, Columbia, MD, U.S.A.
Condizione: New.
Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 265,59
Quantità: 9 disponibili
Aggiungi al carrelloCondizione: New.
Da: moluna, Greven, Germania
EUR 239,03
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Aggiungi al carrelloCondizione: New. Mark Rogge, David R. TaftPreclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regul.
Da: ECOSPHERE, Champs sur marne, Francia
EUR 229,00
Quantità: 1 disponibili
Aggiungi al carrelloCouverture rigide. Condizione: Neuf. 2ème Édition.
EUR 66,37
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Aggiungi al carrelloCondizione: Gut. Zustand: Gut | Sprache: Deutsch | Produktart: Bücher | Keine Beschreibung verfügbar.
Da: CitiRetail, Stevenage, Regno Unito
EUR 17,23
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Aggiungi al carrelloPaperback. Condizione: new. Paperback. Phoenix Rewritten: The Rise of Policy-Driven SecurityBy Mark O. RoggeA single overlooked account. A catastrophic data breach. A race to rebuild trust before the entire company collapses.When a late-night phone call jolts CISO Lauren Reyes from her sleep, she's thrust into the eye of a storm: a devastating cyberattack has compromised millions of patient records at Zenith, one of the nation's largest healthcare providers. But what begins as a technical investigation quickly spirals into a chilling realization-the true threat isn't outside the firewall. It's embedded deep within the architecture of the organization itself.In this gripping corporate techno-thriller, author Mark O. Rogge weaves a suspense-filled narrative that explores the modern crisis of digital trust. As Lauren and her team uncover layer upon layer of neglected service accounts, ghost permissions, and hidden architectural flaws, they discover a concept that could either save or doom the company: Policy Debt.Enter Elias Tran, a mysterious expert with a blueprint for transformation-leveraging Open Policy Agent (OPA) and a revolutionary concept known as policy-as-code. But rebuilding trust means more than just deploying new tools; it means dismantling decades of cultural inertia, breaking down silos, and reimagining how access is defined across every corner of the enterprise.Phoenix Rewritten is a must-read for CISOs, DevSecOps leaders, and technology executives navigating the high-stakes world of security, compliance, and enterprise transformation. Part business thriller, part field manual, it's a visceral story of leadership, failure, and the rising call for policy-driven security in an age where digital trust is everything. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Da: Majestic Books, Hounslow, Regno Unito
EUR 259,90
Quantità: 3 disponibili
Aggiungi al carrelloCondizione: New. pp. 536 Illus. This item is printed on demand.
Lingua: Inglese
Editore: Taylor & Francis, CRC Press, 2009
ISBN 10: 1420084720 ISBN 13: 9781420084726
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 244,70
Quantità: 2 disponibili
Aggiungi al carrelloBuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Preclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regulatory expectations to requirements that support clinical trials. Highlights of the Second Edition include: PharmacokineticsModeling and simulationFormulation and routes of administrationToxicity evaluationsThe assessment of drug absorption and metabolismInterspecies scaling Lead molecule selection and optimization via profilingScreening using in silico and in vitro toxicity evaluations The book also includes case studies on preclinical pharmacokinetic-pharmacodynamic modeling and simulation in drug development, a review of ICH preclinical guidelines, and experimental methods used to study membrane drug transport and metabolism. This guide is a fundamental resource for medicinal chemists, biologists, and other specialists in the drug development sciences. 380 pp. Englisch.
Lingua: Inglese
Editore: Taylor & Francis, CRC Press, 2009
ISBN 10: 1420084720 ISBN 13: 9781420084726
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 267,24
Quantità: 1 disponibili
Aggiungi al carrelloBuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Preclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regulatory expectations to requirements that support clinical trials. Highlights of the Second Edition include: PharmacokineticsModeling and simulationFormulation and routes of administrationToxicity evaluationsThe assessment of drug absorption and metabolismInterspecies scaling Lead molecule selection and optimization via profilingScreening using in silico and in vitro toxicity evaluations The book also includes case studies on preclinical pharmacokinetic-pharmacodynamic modeling and simulation in drug development, a review of ICH preclinical guidelines, and experimental methods used to study membrane drug transport and metabolism. This guide is a fundamental resource for medicinal chemists, biologists, and other specialists in the drug development sciences.