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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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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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Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition

and regulatory concerns. Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition presents in-depth discussions from more;

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Generic Drug Product Development

The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand;

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Generic Drug Product Development

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet;

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Generic Drug Product Development

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet;

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Authorized Generic Drugs

procedures through which independent generic drug companies receive government permission to market their products and resolve patent disputes with;

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Drug Product Development for the Back of the Eye

of administration and delivery systems Noninvasive and continuous drug monitoring Regulatory path to drug product development Clinical endpoints for;

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Pharmacovigilance Medical Writing

Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e;

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Biosimilar Drug Product Development

When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated;

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Pharmaceutical Drug Product Development and Process Optimization

systematic development of drug products with predefined objectives to provide enhanced product and process understanding. This volume presents and;

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Pharmaceutical Practice and Policy

encompasses biologics, drugs, vaccines and natural health products. Patent laws apply to all pharmaceutical products. Thus, the interpretations;

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Generic Drugs

sold as a generic for as little as $30 per month. This book examines the pay-for-delay' program and how drug company pay-offs cost consumers;

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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent;

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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent;

Vergelijkbare producten zoals Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent;

Vergelijkbare producten zoals Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent. Features;

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The Drug Recognition Guide, 2nd Edition

identify the type and use of a generic drug by visually deconstructing its name. Through its creative use of colour-coded drug prefixes and;

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Topical and Transdermal Drug Delivery

scientists, skin product development experts, and those in the cosmetic and personal care industry with practical knowledge and insight into future;

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Generic Drugs

their own products. This book presents an analysis of the innovation and public health issues relating to authorised generic drugs. The book;

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Supercritical Fluid Technology for Drug Product Development

of supercritical fluids to further the development of improved pharmaceutical products-from drug powders for respiratory delivery to drug delivery systems;

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Prescription Drug Pricing Background, Discount Programs and Cost Lowering Strategies

development, regulation of direct-to-consumer advertising, legal restrictions on reimportation, and federal price negotiation. The 340B Drug Pricing;

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Chemical Engineering in the Pharmaceutical Industry

drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design;

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The Future of Pharmaceutical Product Development and Research

Product Development and Research series deepens our understanding of the product development phase of drug discovery and drug development. Each;

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Career Opportunities In Biotechnology And Drug Development

Offers detailed information on over one hundred careers in such areas as regulatory affairs, product development, information management;

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Real-World Evidence in Drug Development and Evaluation

This book concerns use of real world data (RWD) and real world evidence (RWE) to aid drug development across product cycle. RWD are;

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The PA's Complete Guide to Prescribing Drug Therapy 2019

convenient table format. An alphabetical cross-reference index of drugs by generic and brand name, with FDA pregnancy category and controlled drug;

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