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  2. Title 42 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_42_of_the_Code_of...

    CFR Title 42 - Public Health is one of fifty titles comprising the United States Code of Federal Regulations (CFR). Title 42 is the principal set of rules and regulations issued by federal agencies of the United States regarding public health, including respirator rules and regulations moved from CFR Title 30 (including MSHA), to the Public Health Service (including NIOSH and the CDC).

  3. Title 42 of the United States Code - Wikipedia

    en.wikipedia.org/wiki/Title_42_of_the_United...

    Title 42 of the United States Code is the United States Code dealing with public health, social welfare, and civil rights. Parts of Title 42 which formerly related to the US space program have been transferred to Title 51 .

  4. 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.

  5. Intermediate Care Facilities for Individuals with ...

    en.wikipedia.org/wiki/Intermediate_Care...

    According to federal law 42 CFR § 440.150 the purpose of ICD/IIDs is to "furnish health or rehabilitative services to persons with Intellectual Disability or persons with related conditions." [2] The number of individuals living in ICD/IID facilities peaked in 1993 at 147,729 people.

  6. Medical privacy - Wikipedia

    en.wikipedia.org/wiki/Medical_privacy

    Patients are often unaware of the lack of privacy they have as medical processes and forms do not explicitly state the extent of how protected they are. [42] Physicians believe that overall, HIPAA will cause unethical and non-professional mandates that can affect a person's privacy and therefore, they in response have to provide warnings about ...

  7. Clinical Laboratory Improvement Amendments - Wikipedia

    en.wikipedia.org/wiki/Clinical_Laboratory...

    During the retention period, specimens are considered to be part of the medical record and must be kept under a CLIA accredited laboratory to ensure compliant handling and storage conditions. [ 25 ] [ 26 ] If a specimen is sent-out to a non-CLIA biorepository and recalled, the additional testing would not be in compliance. [ 25 ]

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