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Stronger Food and Drug Regulatory Systems Abroad

: Ensuring Safe Foods and Medical Products Through Stronger Regulatory Systems Abroad;

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Ensuring Safe Foods and Medical Products Through Stronger Regulatory Systems Abroad

Medical Products Through Stronger Regulatory Systems Abroad explains that the diversity and scale of imports makes it impractical for U.S. Food;

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Drug Delivery Trends

Realities of Multifunctional Drug Delivery Systems examines the fabrication, optimization, biological aspects, regulatory and clinical success;

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Delivery of Drugs

, optimization, scale-up, biological aspects, regulatory and clinical success of various micro and nano drug delivery systems. The volume covers site and;

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Enhancing Food Safety

. Food and Drug Administration (FDA) oversees monitoring and intervention for 80 percent of the food supply. The U.S. Food and Drug;

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Drug Delivery Aspects

on formulation engineering and related large scale (GMP) manufacturing, regulatory, and functional aspects of drug delivery systems. A;

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Long-Acting Drug Delivery Systems: Pharmaceutical, Clinical, and Regulatory Aspects

Long-Acting Drug Delivery Systems: Pharmaceutical, Clinical, and Regulatory Aspects offers a comprehensive overview of the technical;

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Guidebook for Drug Regulatory Submissions

The high-stakes process of submitting drug documents and applications for regulatory review can be intimidating, particularly for the;

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Nanopharmaceuticals

fabrication, optimization, biological aspects, regulatory and clinical success of wide range of drug delivery carriers. This series reviews;

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Building a National Framework for the Establishment of Regulatory Science for Drug Development

The Food and Drug Administration (FDA) is tasked with ensuring the safety and effectiveness of medicine. FDA's science base must be strong;

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Food Safety

responsibility for food safety rests primarily with the Food and Drug Administration (FDA) and the U.S. Department of Agriculture (USDA). The combined;

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Power, Politics and Pharmaceuticals

? And, what do existing systems of drug regulation reveal the power of transnational pharmaceutical corporations to shape regulatory and other;

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Drug Residues in Foods: Pharmacology

Offers unique data on the physiochemical properties, functions and metabolism, toxicological and pharmacological effects, regulatory;

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The Path from Biomarker Discovery to Regulatory Qualification

history and current regulatory settings in both the US and abroad. This multi-contributed book provides a detailed look at the next step to;

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Conservatism, Consumer Choice, and the Food and Drug Administration during the Reagan Era

In the last quarter of the 20th century, politicians in Washington, as well as interest groups, regulatory policy makers, and drug industry;

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Conservatism, Consumer Choice, and the Food and Drug Administration During the Reagan Era

In the last quarter of the 20th century, politicians in Washington, as well as interest groups, regulatory policy makers, and drug industry;

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Strategies for Reducing Drug and Chemical Residues in Food Animals

veterinary clinical practice and the use of these drugs in food animals with regulatory standards and mitigation practices;

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FDA Drug Approval

The Food and Drug Administration (FDA) oversees the approval and regulation of drugs entering the U.S. market. Two regulatory frameworks;

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Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems

To facilitate the development of novel drug delivery systems and biotechnology-oriented drugs, the need for new excipients to be developed;

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Regulation of Functional Foods and Nutraceuticals

Regulation of Functional Foods and Nutraceuticals: A Global Perspective offers a comprehensive resource for information on regulatory;

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Metabolite Safety in Drug Development

A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental;

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Analytical Method Development and Validation

validation in high-performance liquid chromatography (HPLC) areas. The text presents an overview of Food and Drug Administration (FDA)/International;

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FDA Regulatory Affairs

FDA Regulatory Affairs is a roadmap to prescription drug, biologics, and medical device development in the United States. Written in plain;

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Applications of Polymers in Drug Delivery

polymeric materials can be applied to current, new, and emerging drug delivery applications. Polymers play a crucial role in modulating;

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Drug Delivery Systems

regulatory perspectives. This third edition contains a chapter on nanoscience and technology for drug delivery along with cutting-edge business;

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Modified-Release Drug Delivery Technology

include: modified drug release landscape; academic, regulatory, and intellectual property viewpoints I-vation Sustained Release;

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Handbook of Non-Invasive Drug Delivery Systems

Regulatory Aspects of non-invasive systems and one on FDA guidance for topical nano-drug delivery. Two chapters covering market trends and;

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