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Formulation and Device Lifecycle Management of Biotherapeutics - A Guidance for Researchers and Drug Developers (Paperback)
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Formulation and Device Lifecycle Management of Biotherapeutics - A Guidance for Researchers and Drug Developers (Paperback)
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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. The target audience are multidisciplinary researchers and
drug developers in the pharmaceutical industry, biotech companies,
and academia involved in formulation and device development. This
includes pharmacology and medical experts in charge of generating
nonclinical and clinical data to support approval of novel dosing
regimens, and drug delivery scientists and engineers responsible
for technical particulars of product optimizations. Moreover,
professionals in market access and commercial functions are
expected to benefit from the discussions about the impact of
patient and healthcare provider needs and country-specific
reimbursement models on realizing a truly convenient and cost and
resource efficient drug delivery solution.
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