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Da: Rarewaves.com USA, London, LONDO, Regno Unito
EUR 26,07
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Aggiungi al carrelloPaperback. Condizione: New.
EUR 23,70
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Aggiungi al carrelloCondizione: New.
Editore: Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Da: Majestic Books, Hounslow, Regno Unito
EUR 9,34
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Aggiungi al carrelloCondizione: New.
Editore: Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Da: Books Puddle, New York, NY, U.S.A.
Condizione: New.
Editore: Shashwat Publication
ISBN 10: 9360874868 ISBN 13: 9789360874865
Da: Majestic Books, Hounslow, Regno Unito
EUR 10,31
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Aggiungi al carrelloCondizione: New.
Editore: Shashwat Publication
ISBN 10: 9360874868 ISBN 13: 9789360874865
Da: Books Puddle, New York, NY, U.S.A.
Condizione: New.
Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 23,68
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Aggiungi al carrelloCondizione: New. In.
Editore: Shashwat Publication
ISBN 10: 9360873853 ISBN 13: 9789360873851
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 9,95
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Aggiungi al carrelloCondizione: New.
Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 23,10
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Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 25,19
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Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 34,31
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EUR 34,51
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Aggiungi al carrelloTaschenbuch. Condizione: 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.
EUR 23,11
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Aggiungi al carrelloPaperback. Condizione: New.
EUR 50,24
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Aggiungi al carrelloBuch. Condizione: 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.
Da: PBShop.store US, Wood Dale, IL, U.S.A.
EUR 26,55
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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 23,74
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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: PBShop.store US, Wood Dale, IL, U.S.A.
EUR 38,70
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Aggiungi al carrelloHRD. 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 34,87
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Aggiungi al carrelloHRD. 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.