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Librería: Rarewaves.com USA, London, LONDO, Reino Unido
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de America
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Librería: GreatBookPricesUK, Woodford Green, Reino Unido
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Librería: GreatBookPricesUK, Woodford Green, Reino Unido
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Librería: Grand Eagle Retail, Bensenville, IL, Estados Unidos de America
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Añadir al carritoPaperback. Condición: new. Paperback. Drug Development Roadmap: From Lab Bench to Pharmacy Shelf is a comprehensive, real-world guide to the full lifecycle of pharmaceutical development-from early discovery to commercial launch. Written for scientists, regulatory professionals, formulation experts, and industry newcomers, this resource demystifies the drug development process with clarity and technical depth.Drawing from more than two decades of global industry experience, author Mirela Gorjanu presents a step-by-step framework that spans target identification, preclinical studies, GMP manufacturing, analytical method development, clinical trials, regulatory submissions, and post-marketing surveillance.With Cardiovex-a fictitious case study drug-woven throughout, the book bridges theoretical concepts with practical execution, covering topics such as: Analytical method development (HPLC, LC-MS/MS, dissolution)GMP scale-up, packaging, and stability strategyClinical trials, bioequivalence, and regulatory submission formats (CTD/eCTD)Risk management, pharmacovigilance, and lifecycle controlChange control, serialization, and global pharmacy launch planningAligned with ICH, FDA, EMA, and WHO standards, this reference equips readers to navigate complex regulatory environments and build quality into every phase of development. Whether you're launching a new molecule or reformulating a generic, this roadmap delivers the insights and tools needed to accelerate innovation while ensuring compliance and patient safety. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Librería: PBShop.store UK, Fairford, GLOS, Reino Unido
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Añadir al carritoPAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Librería: Rarewaves.com UK, London, Reino Unido
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Librería: CitiRetail, Stevenage, Reino Unido
EUR 16,68
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Añadir al carritoPaperback. Condición: new. Paperback. Drug Development Roadmap: From Lab Bench to Pharmacy Shelf is a comprehensive, real-world guide to the full lifecycle of pharmaceutical development-from early discovery to commercial launch. Written for scientists, regulatory professionals, formulation experts, and industry newcomers, this resource demystifies the drug development process with clarity and technical depth.Drawing from more than two decades of global industry experience, author Mirela Gorjanu presents a step-by-step framework that spans target identification, preclinical studies, GMP manufacturing, analytical method development, clinical trials, regulatory submissions, and post-marketing surveillance.With Cardiovex-a fictitious case study drug-woven throughout, the book bridges theoretical concepts with practical execution, covering topics such as: Analytical method development (HPLC, LC-MS/MS, dissolution)GMP scale-up, packaging, and stability strategyClinical trials, bioequivalence, and regulatory submission formats (CTD/eCTD)Risk management, pharmacovigilance, and lifecycle controlChange control, serialization, and global pharmacy launch planningAligned with ICH, FDA, EMA, and WHO standards, this reference equips readers to navigate complex regulatory environments and build quality into every phase of development. Whether you're launching a new molecule or reformulating a generic, this roadmap delivers the insights and tools needed to accelerate innovation while ensuring compliance and patient 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.