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This highly engaging guide for clinical researchers 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, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This will be an invaluable resource for basic
Clinical Protocols. --- Ethics. --- Writing. --- Biomedical Research --- Clinical trials. --- Etudes cliniques --- ethics. --- Clinical Protocols --- Proposal writing in medicine --- Human experimentation in medicine --- standards --- ethics --- Moral and ethical aspects --- biomedisch, medisch-wetenschappelijk onderzoek --- onderzoeksprotocol --- recherche biomédicale --- protocole de recherche --- Authorship --- Medical writing --- Controlled clinical trials --- Patient trials of new treatments --- Randomized clinical trials --- Trials, Clinical --- Clinical medicine --- Research --- Medical protocols. --- Clinical algorithms --- Clinical protocols --- Patient care plans --- Plans for patient care --- Protocols in medicine --- Medical records --- Clinical Protocols - standards --- Biomedical Research - ethics --- Human experimentation in medicine - Moral and ethical aspects
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