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FDA in the Twenty-First Century: The Challenges of Regulating Drugs and New Technologies

Amazon.com Price:  $55.87 (as of 12/05/2019 16:48 PST- Details)

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Description

In its decades-long effort to assure the security, efficacy, and security of medicines and other products, the Food and Drug Administration has struggled with issues of funding, proper associations with industry, and the balance between consumer choice and consumer protection. Nowadays, these challenges are compounded by the pressures of globalization, the introduction of novel technologies, and fast-evolving threats to public health. With essays by leading scholars and government and private-industry experts, FDA within the Twenty-First Century addresses perennial and new problems and the improvements the agency can make to raised serve the public good.

The collection features essays on effective regulation in an era of globalization, consumer empowerment, and comparative effectiveness, in addition to questions of data transparency, conflicts of interest, industry responsibility, and innovation policy, all with an emphasis on pharmaceuticals. The book also intervenes within the debate over off-label drug marketing and the right kind role of the FDA before and after a drug goes in the marketplace. Dealing honestly and thoroughly with the FDA’s successes and screw ups, these essays rethink the structure, function, and future of the agency and the effect policy innovations can have on regulatory institutions in a foreign country.

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