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1. |
Record Nr. |
UNINA9910460375303321 |
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Autore |
Cowing Cedric B. |
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Titolo |
Populists, plungers, and progressives : a social history of stock and commodity speculation, 1868-1932 / / Cedric B. Cowing |
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Pubbl/distr/stampa |
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Princeton, New Jersey : , : Princeton University Press, , 1965 |
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©1965 |
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ISBN |
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0-691-04555-0 |
1-4008-7498-X |
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Descrizione fisica |
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1 online resource (307 p.) |
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Collana |
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Princeton Legacy Library ; ; 2366 |
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Disciplina |
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Soggetti |
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Stock exchanges - United States |
Investments - United States |
Electronic books. |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Bibliography: p. 275-283. |
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Nota di contenuto |
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Front matter -- Preface -- Contents -- 1. Agrarians and Commodity Speculators -- 2. Financial Reformers and Progressives -- 3. World War I and the Growth of Speculation -- 4. The Twenties: "Sons of the Wild Jackass" -- 5. The Twenties: Bulls, Bears, and Commentators -- 6. After the 1929 Crash: Investigation, Compromise, Reform -- 7. Conclusion -- Appendix -- Bibliography -- Index |
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Sommario/riassunto |
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From market memoirs, newspapers, financial journals, and Congressional records, the author has woven a narrative describing the political, social, and economic adjustment of the American people to the speculative machinery that developed between 1868 and the New Deal. The book begins with the struggle of Populist legislators, representing stable farmers, to win a Congressional ban of future commodity trading. Congress failed to act, but anti-speculation, a characteristic of Populism, remained important. In the Progressive era, the stock market rivaled the commodity exchanges for attention. Criticism of market practices was rampant as stories of Plungers spread, but no halt came until the crash. Then New Deal philosophy favored the Progressive faction of the anti-speculators. Originally published in 1965.The Princeton Legacy Library uses the latest print- |
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on-demand technology to again make available previously out-of-print books from the distinguished backlist of Princeton University Press. These editions preserve the original texts of these important books while presenting them in durable paperback and hardcover editions. The goal of the Princeton Legacy Library is to vastly increase access to the rich scholarly heritage found in the thousands of books published by Princeton University Press since its founding in 1905. |
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2. |
Record Nr. |
UNINA9910144253403321 |
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Autore |
Tobin Jack (John J.) |
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Titolo |
Medical product regulatory affairs : pharmaceuticals, diagnostics, medical devices / / by John J. Tobin and Gary Walsh |
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Pubbl/distr/stampa |
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Weinheim, [Germany] : , : Wiley-Blackwell, , 2008 |
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©2008 |
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ISBN |
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3-527-64471-7 |
1-281-94710-5 |
9786611947101 |
3-527-62303-5 |
3-527-62304-3 |
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Descrizione fisica |
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1 online resource (299 p.) |
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Disciplina |
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Soggetti |
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Drugs - Law and legislation |
Pharmacy - Law and legislation |
Medical instruments and apparatus - Law and legislation |
Electronic books. |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references at the end of each chapters and index. |
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Nota di contenuto |
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Medical Product Regulatory Affairs; Contents; Preface; 1 The Aims and Structure of Regulations; 2 Regulatory Strategy; 3 Drug Discovery and Development; 4 Non-Clinical Studies; 5 Clinical Trials; 6 Marketing Authorisation; 7 Authorisation of Veterinary Medicines; 8 Variations to |
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the Drug Authorisation Process; 9 Medical Devices; 10 Authorisation of Medical Devices; 11 Good Manufacturing Practice (GMP); 12 Oversight and Vigilance; Index |
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Sommario/riassunto |
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Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field.Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and regulation in the USA. Other topics dealt with include CDER, CBER and marketing and manufacturing licenses, the ICH process and Good Laboratory/Clinical/Manufacturing Practices.Everything pharmacolog |
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