NR599 CHAMERLAIN- INFORMATICS
EXAM WITH 100% CORRECT
ANSWERS 2025/2026
Ethical decision making correct answers >> -Ethical decision
making refers to the process of making informed choices about
ethical dilemmas based on a set of standards differentiating right
from wrong.
-The E-Health Code of Ethics (eHealth code, n.d.), which includes
eight standards for the ethical development of health-related
Internet sites: (1) candor, (2) honesty, (3) quality, (4) informed
consent, (5) privacy, (6) professionalism, (7) responsible
partnering, and (8) accountability.
-the concept of nonmaleficence ("do no harm") will be broadened
to include those individuals and groups whom one may never see
in person, but with whom one will enter into a professional
relationship of trust and care.suggests that both autonomy and
justice are enhanced with universal access to information, but
that tensions may be created in patient-provider relationships as
a result of this access to outside information. Healthcare workers
need to realize that they are no longer the sole providers and
gatekeepers of health-related information; ideally, they should
embrace information empowerment and suggest websites to
patients that contain reliable, accurate, and relevant information
Bioethical standards correct answers >> bioethical decision-
making model centers on the healthcare professional's implicit
agreement with the patient or client (1) autonomy, (2) freedom,
(3) veracity, (4) privacy, (5) beneficence, and (6) fidelity.
, Telehealth correct answers >> Telehealth is still an evolving
technology; while the offsite interventions or contacts often lead
to less time being wasted on non-care-oriented tasks because of
the efficiencies offered by the technology applications, its use
must never be associated with less care. It is also important to
note that nursing activity in telehealth still follows the same best
practice standards as those espoused in conventional care.
FDA Oversight for Medical Devices correct answers >> The
FDA intends to apply its regulatory authorities to select software
applications intended for use on mobile platforms. Given the rapid
expansion and broad applicability of mobile apps, the FDA is
issuing this guidance document to clarify the subset of mobile
apps to which the FDA intends to apply its authority. Many mobile
apps are not medical devices, meaning such mobile apps do not
meet the definition of a device by the FDA. therefore, the FDA
does not regulate them.Some mobile apps may meet the
definition of a medical device but because they pose a lower risk
to the public, the FDA intends to exercise enforcement discretion
over these devices (meaning it will not enforce requirements
under the FD&C Act). One example is a mobile app that makes a
light emitting diode (LED) operate. If the manufacturer intends
the system to illuminate objects generally (i.e., without a specific
medical device intended use), the mobile app would not be
considered a medical device. If, however, through marketing,
labeling, and the circumstances surrounding the distribution, the
mobile app is promoted by the manufacturer for use as a light
source for providers to examine patients, then the intended use of
the light source would be similar to a conventional device such as
an ophthalmoscope.
Privacy correct answers >> According to Healthit.gov (2014)
Protecting Your Health Information, the privacy and security of
patient health information is a top priority for patients and their
families, health care providers and professionals, and the
EXAM WITH 100% CORRECT
ANSWERS 2025/2026
Ethical decision making correct answers >> -Ethical decision
making refers to the process of making informed choices about
ethical dilemmas based on a set of standards differentiating right
from wrong.
-The E-Health Code of Ethics (eHealth code, n.d.), which includes
eight standards for the ethical development of health-related
Internet sites: (1) candor, (2) honesty, (3) quality, (4) informed
consent, (5) privacy, (6) professionalism, (7) responsible
partnering, and (8) accountability.
-the concept of nonmaleficence ("do no harm") will be broadened
to include those individuals and groups whom one may never see
in person, but with whom one will enter into a professional
relationship of trust and care.suggests that both autonomy and
justice are enhanced with universal access to information, but
that tensions may be created in patient-provider relationships as
a result of this access to outside information. Healthcare workers
need to realize that they are no longer the sole providers and
gatekeepers of health-related information; ideally, they should
embrace information empowerment and suggest websites to
patients that contain reliable, accurate, and relevant information
Bioethical standards correct answers >> bioethical decision-
making model centers on the healthcare professional's implicit
agreement with the patient or client (1) autonomy, (2) freedom,
(3) veracity, (4) privacy, (5) beneficence, and (6) fidelity.
, Telehealth correct answers >> Telehealth is still an evolving
technology; while the offsite interventions or contacts often lead
to less time being wasted on non-care-oriented tasks because of
the efficiencies offered by the technology applications, its use
must never be associated with less care. It is also important to
note that nursing activity in telehealth still follows the same best
practice standards as those espoused in conventional care.
FDA Oversight for Medical Devices correct answers >> The
FDA intends to apply its regulatory authorities to select software
applications intended for use on mobile platforms. Given the rapid
expansion and broad applicability of mobile apps, the FDA is
issuing this guidance document to clarify the subset of mobile
apps to which the FDA intends to apply its authority. Many mobile
apps are not medical devices, meaning such mobile apps do not
meet the definition of a device by the FDA. therefore, the FDA
does not regulate them.Some mobile apps may meet the
definition of a medical device but because they pose a lower risk
to the public, the FDA intends to exercise enforcement discretion
over these devices (meaning it will not enforce requirements
under the FD&C Act). One example is a mobile app that makes a
light emitting diode (LED) operate. If the manufacturer intends
the system to illuminate objects generally (i.e., without a specific
medical device intended use), the mobile app would not be
considered a medical device. If, however, through marketing,
labeling, and the circumstances surrounding the distribution, the
mobile app is promoted by the manufacturer for use as a light
source for providers to examine patients, then the intended use of
the light source would be similar to a conventional device such as
an ophthalmoscope.
Privacy correct answers >> According to Healthit.gov (2014)
Protecting Your Health Information, the privacy and security of
patient health information is a top priority for patients and their
families, health care providers and professionals, and the
