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Obtaining informed consent from blood donors and transfusion recipients involves much more than just getting a consent form signed. This comprehensive guideline delves into the ethical and legal basis of the consent doctrine, providing valuable insights for medical professionals.
The consent process is a crucial aspect of both donor and recipient settings. This guideline outlines the essential elements that should be included in the consent process, empowering medical professionals to provide high-quality care.
In the context of informed consent, the roles of the physician directing a phlebotomy, the treating clinician, and the medical directors of the blood bank or transfusion service are critical. This guideline provides clear guidance on their responsibilities, ensuring a collaborative approach to achieving informed consent.
Written by John W. Burch, MD, and Lynne Uhl, MD, for the AABB Scientific Section Coordinating Committee, this informative resource is a must-read for anyone interested in optimizing their consent processes and delivering exceptional patient care.
By exploring the ethical, legal, and practical aspects of informed consent, medical professionals can ensure that their patients receive the highest level of care, while also staying up-to-date with the latest industry guidelines and best practices.
Improve your informed consent processes today and provide the best possible outcomes for your patients.
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