Helps researchers refine and improve the clinical trials process. Material is written from the perspective of a phase I program in oncology; however, this information can be adapted for use in other programs and phases of clinical trials. Includes chapters on the protocol process, regulatory issues, budgets, the enrollment process, treating the patient, data collection, and organizational issues. The author is affiliated with the University of California-Los Angeles. Wire spiral binding. Annotation c. Book News, Inc., Portland, OR (booknews.com)
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Anbieter: medimops, Berlin, Deutschland
Zustand: very good. Gut/Very good: Buch bzw. Schutzumschlag mit wenigen Gebrauchsspuren an Einband, Schutzumschlag oder Seiten. / Describes a book or dust jacket that does show some signs of wear on either the binding, dust jacket or pages. Artikel-Nr. M00763715697-V
Anzahl: 1 verfügbar
Anbieter: moluna, Greven, Deutschland
Zustand: New. KlappentextProvides a practical approach to understanding the components of a clinical research trial as well as the tools to conduct a well-organized study. Designed for those interested in developing or enhancing skills to coordinate a. Artikel-Nr. 898615338
Anzahl: Mehr als 20 verfügbar
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - Provides a practical approach to understanding the components of a clinical research trial as well as the tools to conduct a well-organized study. Designed for those interested in developing or enhancing skills to coordinate all aspects of clinical trials such as regulatory requirements, budgeting, contracts, patient recruitments and participation, and gathering and recording clear, invaluable data. Artikel-Nr. 9780763715694
Anzahl: 2 verfügbar