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Vol. 13, No. 5, May 2017Happy Trials to Research and Patient Privacy in the 21st Century: HIPAA and Beyond By Rachel Abramovitz As we near the end of the second decade of the 21st century, clinical
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Medical researchers who conduct studies or clinical trials involving patients require research and patient privacy.
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Research and patient privacy refers to the protection of sensitive information related to individuals participating in research studies, ensuring their confidentiality and security.
Any individual or organization conducting research involving patient data is required to file research and patient privacy.
Research and patient privacy forms can be filled out by providing detailed information about the study, the type of data collected, and the measures taken to protect patient information.
The purpose of research and patient privacy is to safeguard the confidentiality and privacy of individuals participating in research studies, ensuring their rights are protected.
Information to be reported on research and patient privacy forms includes but is not limited to: study protocols, data collection methods, security measures, and data retention policies.
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