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2. Medical record - Wikipedia

   en.wikipedia.org/wiki/Medical_record

   The medical record serves as the central repository for planning patient care and documenting communication among patient and health care provider and professionals contributing to the patient's care. An increasing purpose of the medical record is to ensure documentation of compliance with institutional, professional or governmental regulation.

3. 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.

4. Health information management - Wikipedia

   en.wikipedia.org/wiki/Health_information_management

   Health information management's standards history is dated back to the introduction of the American Health Information Management Association, founded in 1928 "when the American College of Surgeons established the Association of Record Librarians of North America (ARLNA) to 'elevate the standards of clinical records in hospitals and other medical institutions.'" [3]

5. Case report form - Wikipedia

   en.wikipedia.org/wiki/Case_report_form

   Case report forms contain data obtained during the patient's participation in the clinical trial. Before being sent to the sponsor, this data is usually de-identified (not traceable to the patient) by removing the patient's name, medical record number, etc., and giving the patient a unique study number.

6. More states are requiring patients to give consent for ...

   www.aol.com/news/more-states-requiring-patients...

   A new batch of states are looking to legislate the level of informed consent when it comes to medical students performing pelvic exams for educational purposes on unconscious patients. At least 20 ...

7. Protected health information - Wikipedia

   en.wikipedia.org/wiki/Protected_health_information

   Consent was rarely brought up within the discussion. [12] Because patient privacy is the reason for regulations on PHI, analyzing consumer data can be extremely difficult to come by. Luca Bonomi and Xiaoqian Jiang determined a technique to perform temporal record linkage using non-protected health information data.