Librería: GreatBookPrices, Columbia, MD, Estados Unidos de America
EUR 22,34
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Añadir al carritoCondición: As New. Unread book in perfect condition.
Librería: GreatBookPrices, Columbia, MD, Estados Unidos de America
EUR 23,69
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Añadir al carritoCondición: New.
Librería: Rarewaves.com USA, London, LONDO, Reino Unido
EUR 26,07
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Añadir al carritoPaperback. Condición: New.
Publicado por Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Librería: Majestic Books, Hounslow, Reino Unido
EUR 9,34
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Publicado por Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Librería: Books Puddle, New York, NY, Estados Unidos de America
EUR 13,69
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Publicado por Shashwat Publication
ISBN 10: 9360874868 ISBN 13: 9789360874865
Librería: Majestic Books, Hounslow, Reino Unido
EUR 10,31
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Añadir al carritoCondición: New.
Publicado por Shashwat Publication
ISBN 10: 9360874868 ISBN 13: 9789360874865
Librería: Books Puddle, New York, NY, Estados Unidos de America
EUR 14,62
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Añadir al carritoCondición: New.
Librería: Ria Christie Collections, Uxbridge, Reino Unido
EUR 23,68
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Añadir al carritoCondición: New. In.
Publicado por Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Librería: Biblios, Frankfurt am main, HESSE, Alemania
EUR 9,95
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Añadir al carritoCondición: New.
Librería: GreatBookPricesUK, Woodford Green, Reino Unido
EUR 23,10
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Añadir al carritoCondición: New.
Librería: GreatBookPricesUK, Woodford Green, Reino Unido
EUR 25,19
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Añadir al carritoCondición: As New. Unread book in perfect condition.
Librería: Ria Christie Collections, Uxbridge, Reino Unido
EUR 34,31
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Añadir al carritoCondición: New. In.
EUR 34,51
Cantidad disponible: 2 disponibles
Añadir al carritoTaschenbuch. Condición: Neu. Neuware - The drug discovery and development process is a complex, multi-faceted journey that begins with the identification of potential therapeutic targets and culminates in the approval and marketing of new medications. This process involves several critical stages, including the discovery phase, preclinical research, clinical trials, and regulatory approval. During the preclinical stage, rigorous pre-formulation studies assess the organoleptic properties, purity, impurity profiles, particle size, shape, surface area, and solubility of drug candidates. These studies are essential for understanding the physicochemical characteristics of the drug and for developing methods to enhance solubility, such as using surfactants or co-solvents. The transition from laboratory-scale to commercial-scale production, known as pilot plant scale-up, requires careful planning, design, and execution to ensure that the manufacturing processes are scalable and that the quality and stability of the drug are maintained. Pharmaceutical packaging plays a crucial role in protecting the drug product, ensuring its stability, and facilitating its safe and effective use. Packaging materials must be carefully selected, evaluated, and tested for quality control to meet regulatory standards. Technology transfer from research and development to production involves optimizing processes, ensuring consistent product quality, and thorough documentation to support regulatory submissions.
Librería: Rarewaves.com UK, London, Reino Unido
EUR 23,11
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Añadir al carritoPaperback. Condición: New.
EUR 50,24
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Añadir al carritoBuch. Condición: Neu. Neuware - The drug discovery and development process is a complex, multi-faceted journey that begins with the identification of potential therapeutic targets and culminates in the approval and marketing of new medications. This process involves several critical stages, including the discovery phase, preclinical research, clinical trials, and regulatory approval. During the preclinical stage, rigorous pre-formulation studies assess the organoleptic properties, purity, impurity profiles, particle size, shape, surface area, and solubility of drug candidates. These studies are essential for understanding the physicochemical characteristics of the drug and for developing methods to enhance solubility, such as using surfactants or co-solvents. The transition from laboratory-scale to commercial-scale production, known as pilot plant scale-up, requires careful planning, design, and execution to ensure that the manufacturing processes are scalable and that the quality and stability of the drug are maintained. Pharmaceutical packaging plays a crucial role in protecting the drug product, ensuring its stability, and facilitating its safe and effective use. Packaging materials must be carefully selected, evaluated, and tested for quality control to meet regulatory standards. Technology transfer from research and development to production involves optimizing processes, ensuring consistent product quality, and thorough documentation to support regulatory submissions.
Librería: PBShop.store US, Wood Dale, IL, Estados Unidos de America
EUR 26,55
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Añadir al carritoPAP. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Librería: PBShop.store UK, Fairford, GLOS, Reino Unido
EUR 23,74
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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: PBShop.store US, Wood Dale, IL, Estados Unidos de America
EUR 38,70
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Añadir al carritoHRD. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Librería: PBShop.store UK, Fairford, GLOS, Reino Unido
EUR 34,87
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Añadir al carritoHRD. 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.