121,31 €
134,79 €
-10% with code: EXTRA
Ethical Considerations When Preparing a Clinical Research Protocol
Ethical Considerations When Preparing a Clinical Research Protocol
121,31
134,79 €
  • We will send in 10–14 business days.
Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and assent documents, how to get protocols approved, special populations, confidentiality issues, and the reporting of adverse events. The boo…
  • Publisher:
  • ISBN-10: 0123869358
  • ISBN-13: 9780123869357
  • Format: 15.2 x 22.9 x 2 cm, softcover
  • Language: English
  • SAVE -10% with code: EXTRA

Ethical Considerations When Preparing a Clinical Research Protocol (e-book) (used book) | bookbook.eu

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Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and assent documents, how to get protocols approved, special populations, confidentiality issues, and the reporting of adverse events. The book's valuable appendix includes a listing of web resources about research ethics, along with a glossary, making it an invaluable resource for scientists collaborating in clinical trials, physician investigators, clinical research fellows, and more.

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  • Author: Evan DeRenzo
  • Publisher:
  • ISBN-10: 0123869358
  • ISBN-13: 9780123869357
  • Format: 15.2 x 22.9 x 2 cm, softcover
  • Language: English English

Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and assent documents, how to get protocols approved, special populations, confidentiality issues, and the reporting of adverse events. The book's valuable appendix includes a listing of web resources about research ethics, along with a glossary, making it an invaluable resource for scientists collaborating in clinical trials, physician investigators, clinical research fellows, and more.

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