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  • Langue : anglais

    Edité par ThinkPlus Pharma Publications, 2026

    8198765719 / 9788198765710

    • Couverture souple

    Vendeur : California Books, Miami, FL, Etats-UnisCalifornia Books

    Vendeur avec une évaluation de 5 étoiles
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    Etat: Neuf

    EUR 21,12

    EUR 2,67 expédition 
    Expédition nationale : Etats-Unis

    Quantité disponible : Plus de 20 disponibles

    Etat : New.

  • Langue : anglais

    Edité par Amazon Digital Services LLC - Kdp Mai 2026, 2026

    8198765719 / 9788198765710

    • Couverture souple

    Vendeur : AHA-BUCH GmbH, Einbeck, AllemagneAHA-BUCH GmbH

    Vendeur avec une évaluation de 5 étoiles
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    Etat: Neuf

    EUR 29,10

    EUR 35,00 expédition 
    Expédition depuis Allemagne vers Etats-Unis

    Quantité disponible : 2 disponibles

    Taschenbuch. Etat : Neu. Neuware - Essentials of Clinical Trials and Cancer Drug Development is a detailed guide designed for students, researchers, and emerging professionals exploring the fields of pharmaceutical science, data integrity, and patient safety. In an era where medical breakthroughs depend as much on robust data management as they do on biological innovation, this textbook provides a clear, structured roadmap through the entire clinical trial lifecycle. Focused specifically on the high-stakes field of oncology, the book explains about the unique challenges of cancer drug development from phase I dose-escalation and biomarker-driven trials to advanced survival analysis and regulatory submission. Readers will explore critical topics such as Good Clinical Practice (GCP), the role of Artificial Intelligence in data monitoring, and the ethical imperatives of the Declaration of Helsinki. Authors Dr. Sambasiva Rao Tummala and Dr. Naveena Gorrepati offer an indispensable resource for those dedicated to safeguarding public health and advancing the next generation of life-saving cancer therapies by blending rigorous statistical methodology with practical insights into pharmacovigilance and drug safety.…

  • Langue : anglais

    Edité par Thinkplus Pharma Publications, 2026

    8198765719 / 9788198765710

    • Couverture souple
    • impression à la demande

    Vendeur : Grand Eagle Retail, Bensenville, IL, Etats-UnisGrand Eagle Retail

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    Etat: Neuf

    EUR 22,25

     Frais de port gratuits 
    Expédition nationale : Etats-Unis

    Quantité disponible : 1 disponible

    Paperback. Etat : new. Paperback. Essentials of Clinical Trials and Cancer Drug Development is a detailed guide designed for students, researchers, and emerging professionals exploring the fields of pharmaceutical science, data integrity, and patient safety. In an era where medical breakthroughs depend as much on robust data management as they do on biological innovation, this textbook provides a clear, structured roadmap through the entire clinical trial lifecycle. Focused specifically on the high-stakes field of oncology, the book explains about the unique challenges of cancer drug development from phase I dose-escalation and biomarker-driven trials to advanced survival analysis and regulatory submission. Readers will explore critical topics such as Good Clinical Practice (GCP), the role of Artificial Intelligence in data monitoring, and the ethical imperatives of the Declaration of Helsinki. Authors Dr. Sambasiva Rao Tummala and Dr. Naveena Gorrepati offer an indispensable resource for those dedicated to safeguarding public health and advancing the next generation of life-saving cancer therapies by blending rigorous statistical methodology with practical insights into pharmacovigilance and drug safety. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

  • Langue : anglais

    Edité par Thinkplus Pharma Publications, 2026

    8198765719 / 9788198765710

    • Couverture souple
    • impression à la demande

    Vendeur : PBShop.store US, Wood Dale, IL, Etats-UnisPBShop.store US

    Vendeur avec une évaluation de 5 étoiles
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    Etat: Neuf

    EUR 22,26

     Frais de port gratuits 
    Expédition nationale : Etats-Unis

    Quantité disponible : Plus de 20 disponibles

    PAP. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

  • Langue : anglais

    Edité par Thinkplus Pharma Publications, 2026

    8198765719 / 9788198765710

    • Couverture souple
    • impression à la demande

    Vendeur : PBShop.store UK, Fairford, GLOS, Royaume-UniPBShop.store UK

    Vendeur avec une évaluation de 5 étoiles
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    Etat: Neuf

    EUR 19,94

    EUR 4,96 expédition 
    Expédition depuis Royaume-Uni vers Etats-Unis

    Quantité disponible : Plus de 20 disponibles

    PAP. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

  • Langue : anglais

    Edité par Thinkplus Pharma Publications, 2026

    8198765719 / 9788198765710

    • Couverture souple
    • impression à la demande

    Vendeur : CitiRetail, Stevenage, Royaume-UniCitiRetail

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    Etat: Neuf

    EUR 23,94

    EUR 44,13 expédition 
    Expédition depuis Royaume-Uni vers Etats-Unis

    Quantité disponible : 1 disponible

    Paperback. Etat : new. Paperback. Essentials of Clinical Trials and Cancer Drug Development is a detailed guide designed for students, researchers, and emerging professionals exploring the fields of pharmaceutical science, data integrity, and patient safety. In an era where medical breakthroughs depend as much on robust data management as they do on biological innovation, this textbook provides a clear, structured roadmap through the entire clinical trial lifecycle. Focused specifically on the high-stakes field of oncology, the book explains about the unique challenges of cancer drug development from phase I dose-escalation and biomarker-driven trials to advanced survival analysis and regulatory submission. Readers will explore critical topics such as Good Clinical Practice (GCP), the role of Artificial Intelligence in data monitoring, and the ethical imperatives of the Declaration of Helsinki. Authors Dr. Sambasiva Rao Tummala and Dr. Naveena Gorrepati offer an indispensable resource for those dedicated to safeguarding public health and advancing the next generation of life-saving cancer therapies by blending rigorous statistical methodology with practical insights into pharmacovigilance and drug safety. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…