Description - Writing Clinical Research Protocols by Evan DeRenzo
A practical guide for clinical researchers that aims to improve their skills in the understanding of the ethical requirements for the design and conduct of clinical research. Includes information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocals approved, special populations, confidentiality issues, and the reporting of adverse events. Appendices include internet resources, grant writing tips, as well as advice on subject recruitment and budget considerations.
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Ethical Considerations When Preparing a Clinical Research Protocol
