Informed consent

Xem 1-20 trên 94 kết quả Informed consent
  • Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Ethical issues in implementation research: a discussion of the problems in achieving informed consent

    pdf8p panasonic03 17-12-2011 29 3   Download

  • Malware: software designed to infiltrate or damage a computer system without the owner's informed consent Spyware: software designed to intercept or take partial control over the user's interaction with the computer, without the user's informed consent secretly monitors the user's behavior collect various types of personal information

    pdf33p trinhvietnambk 29-05-2013 25 3   Download

  • Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học General Psychiatry cung cấp cho các bạn kiến thức về ngành y đề tài: Informed consent: time for more transparency...

    pdf2p thulanh14 19-10-2011 21 2   Download

  • Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về ngành y học đề tài: Research in critically ill patients: standards of informed consent...

    pdf2p coxanh_3 25-10-2011 23 2   Download

  • Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Tailoring the process of informed consent in genetic and genomic research

    pdf7p panasonic02 15-12-2011 24 2   Download

  • Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về ngành y học đề tài: Do chiropractic college faculty understand informed consent: a pilot study...

    pdf8p coxanh_5 28-10-2011 27 1   Download

  • (BQ) Part 1 book "Ethical issues in anesthesiology and surgery" presents the following contents: Informed consent - Pediatric patients, adolescents and emancipated minors; informed consent and the disclosure of surgeon experience; pediatric patients do not resuscitate decisions; ethical care of the children of jehovah’s witnesses; fatigue and the care of patients,...

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  • Patients provide valid informed consent to a treatment or a diagnostic procedure if they have sufficient capacity, have been given appropriate information, and give consent freely without coercion or undue influence. When a patient’s capacity for treatment consent is in doubt, a clinician must determine whether the patient indeed has the capacity. It is a common reason behind requests for psychiatric consultations in a general hospital (Appelbaum, 2007).

    pdf216p crius75 09-01-2013 28 2   Download

  • Clinical trials enable scientific discoveries to advance patient care, and they also inform and guide subsequent research. The National Cancer Institute (NCI) supports the largest U.S. network of clinical trials of any type, of which the largest component is the Clinical Trials Cooperative Group Program (informally known as the Cooperative Group Program). It currently comprises 10 Groups that involve more than 3,100 institutions and 14,000 investigators who enroll more than 25,000 patients in clinical trials each year.

    pdf123p tom_123 15-11-2012 21 1   Download

  • The process of informed consent is a well established medical practice which has its roots in ethics and law. The requirement to obtain informed consent is based on the ethical principle of self determination and is strengthened in application by both statutory and case law. As a general rule, with few exceptions, and endoscopist is required to obtain informed consent prior to the performance of any endoscopic procedure.

    pdf263p crazy_sms 07-05-2012 23 8   Download

  • Điều 15 của CBD Chủ quyền của quốc gia về nguồn gen Các bên tạo điều kiện thuận lợi để tiếp cận nguồn gen Việc tiếp cận phải dựa trên nguyên tắc Nhất trí/thỏa thuận thông báo trước(PIC- Prior Informed Consent) và Các điều khoản đồng thuận(MAT-mutually agreed terms) Các bên áp dung các biện pháp để chia sẻ lợi ích trên cơ sở Các điều khoản đồng thuận

    ppt20p ktouch_12 25-06-2013 48 8   Download

  • The American Society for Reproductive Medicine (ASRM) is the specialty society for physicians that focus on infertility. The organization has a Practice Committee that issues regular reports, including guidelines on minimal standards for providing ART, informed consent, and on the number of embryos to be transferred in IVF procedures. The guidelines are distributed to all members of ASRM, are published in the Society's journal, Fertility and Sterility, and are available to the public on ASRM's website (

    pdf13p le_minh_nha 25-12-2012 20 7   Download

  • The use of complementary medicine has mushroomed over the last decade. Along with the increased popularity there’s been an increase in the number of practitioners who practise complementary therapies either as their primary discipline or as a ‘complement’ to their own discipline, such as nursing or medicine. With an increasing acceptance by the public and by mainstream healthcare professionals, practitioners of complementary medicine are being asked to provide evidence of the effectiveness and safety of their therapies.

    pdf206p cronus75 18-01-2013 22 7   Download

  • The aspirator should be aware of the pertinent history and clinical information, significant radiological studies and the clinical question that FNAB may answer. The procedure as well as the minor complications of bruising and bleeding should be explained to the patient. Site-specific complications for deep needle aspiration biopsy should be described to the patient if image guided FNAB is performed. Informed consent should be obtained from the patient, guardian or legal representative.

    pdf235p le_minh_nha 18-12-2012 27 6   Download

  • Participants should be informed that they are free to withdraw from the research at any time. Participants should be informed of the degree of confidentiality that will be maintained in the study. Informed consent of parents or guardians and, where practical, of children should be obtained in research involving children.

    pdf11p connicquy 20-12-2012 22 6   Download

  • We are grateful to everyone who attended the panel’s first meet- ing and provided perspectives on issues of human research participant protection in the social, behavioral, and economic sciences (SBES). We acknowledge the wealth of information that we obtained from web- sites of private and public organizations and from previous surveys of the review process for research with human participants (see the appendices).

    pdf277p banhkem0908 24-11-2012 29 5   Download

  • As the market leader in digital signage, NEC offers a large selection of powerful digital signage solutions that can provide reliable outstanding images over long periods of use. Digital Signage can serve several purposes such as informing, entertaining or providing a purchasing incentive. For instance, a public display with tantalising content placed above a concession stand can boost sales of popcorn, cola and other items.

    pdf0p khanhchilam 01-04-2013 27 5   Download

  • Between December 2003 and December 2007, a total of 222 radical transurethral resection of prostate cancer were performed under spinal anesthesia in 170 patients with clinical stages of T1 or T2. Clinical stages were determined according to the UICC TNM staging system of 1997. We informed the patients that the procedure was not a current standard radical method of management, and those who refused this procedure were excluded from the study. We also excluded patients with serious comorbidities that might affect their lives by standard TURP.

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  • Women with mental disabilities should be involved in decision-making about their reproductive rights to the fullest extent allowed by their capacities. To the degree that a woman can give her informed consent, she is entitled to do so. At the same time, women with mental disabilities may possess particular vulnerabilities that entitle them to heightened protection from sexual abuse and other forms of exploi- tation.

    pdf11p ut_hai_can 25-12-2012 19 4   Download

  • s outlined in the section on advertising Facebook’s policy is that it does not allow the serving of ads based on the use of sensitive data as defined under EU law. In practice, however, it does seem that it is possible to use such information as contained in a profile. In this respect, it is not inappropriate for FB-I to claim legitimate interests for the processing of profile, interest and ‘like’ information entered by a user if it were considered that consent would not be a sufficiently robust basis for such processing. Regardless, there needs to be...

    pdf54p tay_thi_le 19-02-2013 25 4   Download


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