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2. Informed consent - Wikipedia

   en.wikipedia.org/wiki/Informed_consent

   Informed consent is a principle in medical ethics, medical law, media studies, and other fields, that a person must have sufficient information and understanding before making decisions about accepting risk, such as their medical care. Pertinent information may include risks and benefits of treatments, alternative treatments, the patient's role ...

3. List of PDF software - Wikipedia

   en.wikipedia.org/wiki/List_of_PDF_software

   Open-source Java reporting tool that can write to screen, printer, or into PDF, HTML, Microsoft Excel, RTF, ODT, comma-separated values and XML files. libHaru: ZLIB/LIBPNG: Open-source, cross-platform C library to generate PDF files. OpenPDF: GNU LGPLv3 / MPLv2.0: Open source library to create and manipulate PDF files in Java.

4. Sumatra PDF - Wikipedia

   en.wikipedia.org/wiki/Sumatra_PDF

   The Sumatra PDF Viewer is a tiny open source portable reader that opens PDF's in the blink of an eye. Bloat and startup time is a major drawback to Adobe Reader, so we fled to the faster arms of Foxit Reader long ago. However, at 850KB, Sumatra is way slimmer than FoxIt. ^ Anders Ingeman Rasmussen (2008).

5. Dynamic consent - Wikipedia

   en.wikipedia.org/wiki/Dynamic_consent

   Dynamic consent is an approach to informed consent that enables on-going engagement and communication between individuals and the users and custodians of their data. It is designed to address the many issues that are raised by the use of digital technologies in research and clinical care that enable the wide-scale use, linkage, analysis and integration of diverse datasets and the use of AI and ...

6. Informed Consent in Medical Research - Wikipedia

   en.wikipedia.org/wiki/Informed_Consent_in...

   978-0-727-91486-6. Informed Consent in Medical Research is a medical textbook on medical ethics, authored by Jeffrey S. Tobias and Len Doyal, and published by Wiley in 2001. It was produced in response to the debates between the authors in 1997, following the response to the 1990's British Medical Journal publications of studies in which ...

7. Informed assent - Wikipedia

   en.wikipedia.org/wiki/Informed_assent

   In adult medical research, the term informed consent is used to describe a state whereby a competent individual, having been fully informed about the nature, benefits and risks of a clinical trial, agrees to their own participation. National authorities define certain populations as vulnerable and therefore unable to provide informed consent ...