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  2. Protected health information - Wikipedia

    en.wikipedia.org/wiki/Protected_health_information

    There are many forms of PHI, with the most common being physical storage in the form of paper-based personal health records (PHR). Other types of PHI include electronic health records, wearable technology, and mobile applications. In recent years, there has been a growing number of concerns regarding the safety and privacy of PHI.

  3. Health Insurance Portability and Accountability Act - Wikipedia

    en.wikipedia.org/wiki/Health_Insurance...

    Health Insurance Portability and Accountability Act of 1996; Other short titles: Kassebaum–Kennedy Act, Kennedy–Kassebaum Act: Long title: An Act To amend the Internal Revenue Code of 1986 to improve portability and continuity of health insurance coverage in the group and individual markets, to combat waste, fraud, and abuse in health insurance and health care delivery, to promote the use ...

  4. Privacy policy - Wikipedia

    en.wikipedia.org/wiki/Privacy_policy

    The Health Insurance Portability and Accountability Act (HIPAA) privacy rules [22] requires notice in writing of the privacy practices of health care services, and this requirement also applies if the health service is electronic. [23]

  5. ANSI 834 Enrollment Implementation Format - Wikipedia

    en.wikipedia.org/wiki/ANSI_834_Enrollment...

    The X12 834 EDI Enrollment Implementation Format is a standard file format in the United States for electronically exchanging health plan enrollment data between employers and health insurance carriers.

  6. Medical privacy - Wikipedia

    en.wikipedia.org/wiki/Medical_privacy

    The government is exempted from privacy rules regarding national security. HIPAA additionally allows the authorization of protected health information (PHI) in order to aid in threats to public health and safety as long as it follows the good faith requirement - the idea that disclosing of information is necessary to the benefit of the public. [45]

  7. Title 21 CFR Part 11 - Wikipedia

    en.wikipedia.org/wiki/Title_21_CFR_Part_11

    A predicate rule is any requirement set forth in the Federal Food, Drug and Cosmetic Act, the Public Health Service Act, or any FDA regulation other than Part 11. [ 3 ] The rule also applies to submissions made to the FDA in electronic format (e.g., a New Drug Application ) but not to paper submissions by electronic methods (i.e., faxes ).

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