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Formulation and Device Lifecycle Management of Biotherapeutics: A Guidance for Researchers and Drug Developers
Sobre Formulation and Device Lifecycle Management of Biotherapeutics: A Guidance for Researchers and Drug Developers
"Today, the pressure on healthcare costs and resources is increasing, and especially for biopharmaceuticals that require parenteral administration, the inherent complex and invasive dosing procedure adds to the demand for efficient medical management. In light of the COVID-19 pandemic the value of drug delivery technologies in enabling a flexible care setting is broadly recognized. In such a setting, patients and their caregivers can choose the place of drug administration based on individual preferences and capabilities. This includes not only dosing in the clinic but also supervised at-home dosing and self-administration for eligible patients. Formulation and Device Lifecycle Management of Biotherapeutics: A Guidance for Researchers and Drug Developers covers the various aspects of improving drug delivery of biological medicines with the ultimate goal to reduce dosing complexity associated with parenteral administration and, thus, enhance patient experience and drug administration-related healthcare capacity." --
¿Cuántas páginas tiene Formulation and Device Lifecycle Management of Biotherapeutics: A Guidance for Researchers and Drug Developers?
Esta edición de Formulation and Device Lifecycle Management of Biotherapeutics: A Guidance for Researchers and Drug Developers tiene 214 páginas. El tiempo para terminarlo depende de cuántas páginas leas al día.
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