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Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics

Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the;

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Novel Approaches and Strategies for Biologics, Vaccines and Cancer Therapies

challenges involved with the development of novel formulations of biologics, vaccines and cancer therapy. This thorough reference on the latest;

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Biosimilar and Interchangeable Biologics

overall reduction time in costs and development. Biosimilars and Interchangeable Biologics: From Cell Line to Commercial Launch covers the;

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Handbook of Biologics & Biosimilars in Dermatology

of life with biologic therapy, and the book concludes with discussion on future developments and the use of small molecule treatment. Key;

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Biosimilars and Interchangeable Biologics

reduction time in costs and development. Part of a two-volume set that covers varying aspects of biosimilars, Biosimilars and Interchangeable;

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Biologics, Biosimilars, and Biobetters

A comprehensive primer and reference, this book provides pharmacists and health practitioners the relevant science and policy concepts;

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A Comprehensive Guide to Toxicology in Nonclinical Drug Development

understanding of all aspects of nonclinical toxicology in the development of small molecules and biologics. This updated edition has been reorganized;

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Biosimilars and Interchangeable Biologics

reduction time in costs and development. Part of a two-volume set that covers varying aspects of biosimilars, Biosimilars and Interchangeable;

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Biosimilars and Interchangeable Biologics

reduction time in costs and development. Part of a two-volume set that covers varying aspects of biosimilars, Biosimilars and Interchangeable;

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Adme And Translational Pharmacokinetics / Pharmacodynamics O

development and compares innovator biologics with biosimilar biologics and small molecules with biologics, giving a lessons-learned perspective;

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Progress in Medical Research

prescription drug topics covered are federally funded research and development, regulation of direct-to-consumer advertising, legal restrictions on;

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Safety of Biologics Therapy: Monoclonal Antibodies, Cytokines, Fusion Proteins, Hormones, Enzymes, Coagulation Proteins, Vaccines, Botulinum Toxins

; enzymes; proteins involved in blood-clotting, homeostasis and thrombosis; vaccines; botulinum neurotoxins; and, more recently, biosimilar;

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Lyophilized Biologics and Vaccines

This book provides a detailed account of the most recent developments, challenges and solutions to seamlessly advance and launch a;

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Biological Drug Products

segment of the pharmaceutical industry. Contributing authors discuss the development process, safety and clinical assessments, manufacturing;

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Combined Vaccines and Simultaneous Administration

advances and regulatory issues bearing on the development of combination vaccines and vaccines for simultaneous administration are discussed. The;

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Safety of Biologics Therapy

; enzymes; proteins involved in blood-clotting, homeostasis and thrombosis; vaccines; botulinum neurotoxins; and, more recently, biosimilar;

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Continuous Manufacturing for the Modernization of Pharmaceutical Production

manufacturing techniques to produce biologics such as enzymes, monoclonal antibodies, and vaccines. The participants also discussed specific challenges;

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Bone Grafts, Bone Graft Substitutes, and Biologics in Foot and Ankle Surgery, An Issue of Foot and Ankle Clinics of North America

-PDGF; B2-A polypeptide in foot ankle fusion; Adipose-derived msc in hindfoot fusion; Polyvinyl for hallux rigidis; New development of novel;

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The Challenge of CMC Regulatory Compliance for Biopharmaceuticals

the CMC regulatory compliance of biopharmaceuticals; also the application of biosimilars has been developed in Europe and is under development;

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Drug-Drug Interactions for Therapeutic Biologics

focuses on the theoretical and practical aspects of DDIs assessments for therapeutic biologics in drug development. The book addresses the complex;

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Generic Drug Product Development

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;

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Biologics in General Medicine

dermatology and neurology is described in detail and summarized in treatment algorithms. Shorter sections on biologic biotechnology as well as safety;

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Generic Drug Product Development

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;

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Biologics, A History Of Agents Made From Living Organisms In

The use of biologics - drugs made from living organisms - has raised specific scientific, industrial, medical and legal issues. The essays;

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Infection and Malignancy in Rheumatic Diseases, An Issue of Rheumatic Disease Clinics of North America

This issue of Rheumatic Disease Clinics will include articles such as: Vaccines and Biologics- efficacy and toxicity; Improving Vaccine;

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Biologics, A History of Agents Made From Living Organisms in the Twentieth Century

The use of biologics - drugs made from living organisms - has raised specific scientific, industrial, medical and legal issues. The essays;

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Biologics in Otolaryngology, An Issue of Otolaryngologic Clinics of North America

This issue of Otolaryngologic Clinics, guest edited by Drs. Sarah K. Wise, Ashkan Monfared, and Nicole C. Schmitt is devoted to;

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