1. Ethical Medical Data Donation: A Pressing Issue I. Conceptualising the Ethics of Medical Data Donation II. Governance and Regulation of Medical Data Donation III. Implementing Ethical Medical Data Donation IV. An Ethical Code for Posthumous Medical Data Donation ...
Anandh, UrmilaPhadke, K. D., & Anandh, U. (2002). The ethics of organ donation. Journal of the College of Physicians and Surgeons Pakistan JCPSP, 17(1), 2561; author reply 2561. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/9536539...
Huang Jiefu (Chairman of China human organdonation and Transplantation Committee and President of China organ transplantation Development Foundation):"On Nov14, British Medical Association published an article wrote by an Israel so-called "scollar", on BMC Ethics. The article violates basic scientific ...
He had to complete a medical records keeping course, an ethics course, and a clinician patient communication course. The most important stipulation is that he could not practice in a solo practice. In fact, he could not practice at all without being monitored by a board-certified doctor ...
to analyse selected empirical quantitative and qualitative studies as well as theoretical ethics studies about living organ donation (“bottom-up-strategy”) regarding their use of empirical data and ethical concepts, and if they reflected upon that relationship; (ii) to study, present and criticall...
Medical staff must report patients with brain death to the Agence de la Biomédecine, the national organization that handles procedures involving cells, tissues, and organs. An organ-procurement coordinator then completes a detailed evaluation of the patient to determine suitability for organ donation. ...
Before submitting the study to the two ethics committees (Novara Intercompany Ethics Committee and Northumbria University Ethics Committee), we considered the existing ethical frameworks for using biological samples (or their derivatives) taken from deceased subjects. In particular, we examined the issue ...
Appropriate donor informed consent for research use was obtained according to procedures approved by HQT's Ethics Committee and the Spanish Agency of Medicines and Medical Devices (AEMPS). Show abstract Final results of a phase I–II trial using ex vivo expanded autologous Mesenchymal Stromal Cells ...
To achieve this goal, oversight can enforce and monitor the safety, security, ethics of SaMDs at every stage of conceptualization, development, and deployment.88,99 Another highly important regulatory aspect pertains to information security and the nondiscriminatory use of AI for RD diagnosis and ...
Binding research policy documents in most countries today are the result of extensive debates about the ethics of clinical research, exploitation in non-therapeutic research in the global south and other such issues. The introduction of medical aid in dying in an ever-growing number of jurisdictions...