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2. Case report form - Wikipedia

   en.wikipedia.org/wiki/Case_report_form

   A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. [1] The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.

3. Medical writing - Wikipedia

   en.wikipedia.org/wiki/Medical_writing

   Regulatory documents can be huge and are formulaic. They include clinical study protocols, clinical study reports, patient informed consent forms, investigator brochures and summary documents (e.g. in Common Technical Document [CTD] format) that summarize and discuss the data a company gathers in the course of developing a medical product.

4. Informed consent - Wikipedia

   en.wikipedia.org/wiki/Informed_consent

   Example of informed consent document from the PARAMOUNT trial. 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.

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. Promoting Healthy Choices: Information vs. Convenience - HuffPost

   images.huffingtonpost.com/2012-12-21-promoting...

   recent article, George Loewenstein et al. (2007) document the ways in which asymmetrical paternalism can be used to change health behaviors and argue that the standard economic approach of simply providing more information fails to exploit what we know about human motivation, self-control and behavioral change.

7. Research participant - Wikipedia

   en.wikipedia.org/wiki/Research_participant

   A research participant, also called a human subject or an experiment, trial, or study participant or subject, is a person who voluntarily participates in human subject research after giving informed consent to be the subject of the research. A research participant is different from individuals who are not able to give informed consent, such as ...