Another comment argued that federal and state police should be able to obtain personal medical records only with
the informed consent of an individual.
Or if there is no other ground, the free and
informed consent of the individual.»
CREA's Privacy Policy requires that the collection of such information by the Board / Association be done with
the informed consent of the individual.
Not exact matches
So should we ask the Buddists to get the
informed consent of ALL descendents
of an
individual before they start to worship that
individual after he / she has died?
Should Mormons have to get the
informed consent of ALL descendents
of an
individual before believing he / she has an opportunity to accept baptism after this life?
Should we ask Taoists to get the
informed consent of ALL descendents
of an
individual before they start believing that
individual has reincarnated as a dog after he / she has died?
Except for the prudent correction
of an imminent danger, I will neither treat any patient nor carry out any research on any human being without the valid
informed consent of the subject or the appropriate legal protector thereof, understanding that research must have as its purpose the furtherance
of the health
of that
individual.
In other words,
informed consent REQUIRES enumeration and disclosure
of risks SPECIFIC to the
individual patient's diagnosis and proposed treatment.
The idea that personal data collected for one purpose can't be used for another without the
individual's
informed consent is the cardinal principle
of data protection.
Self - monitoring
of blood glucose People with Type 1 and Type 2 diabetes should have access to self - monitoring
of blood glucose (SMBG) based on
individual clinical need, type
of diabetes, personal circumstances and
informed consent - not on ability to pay..
Almost all other libertarian ideals (freedom
of contracts, autonomous judgement,
informed consent,
individual freedom, labor theory
of property, etc.) are philosophically derived from this principle.
The same goes for expectations about who owns or controls ideas, data, and writings; what constitutes conflict
of interest and
informed consent; what responsibilities
individuals have if they observe wrongdoing; and other complex issues that arise in scientific research.
The value placed on
individual autonomy varies in different cultures, so the primacy that it receives in the context
of public health planning and decision making, and the role
of informed consent, might differ between countries [91], [92].
Before a single child's information is turned over to any 3rd party, policymakers should give assurance to parents and educators that no harm will come to Tennessee school children by adopting the following principles: The state and districts should be required to publish any and all existing data sharing agreements in printed and electronic form, and include a thorough explanation
of its purpose and provisions, and make it available to parents and local school authorities statewide; The Department
of Education should hold hearings throughout the state or testify before the legislature to explain any existing data agreement, and answer questions from the public or their representatives, obtain
informed comment, and gauge public reaction; All parents should have the right to be notified
of the impending disclosure
of their children's data, and provide them with a right to
consent or have the right to withhold their children's information from being shared; The state should have to define what rights families or
individuals will have to obtain relief if harmed by improper use or release
of their child's private information, including how claims can be made; and finally, any legislation must ensure that the privacy interest
of public school children and their families are put above the interests
of any 3rd Party and its agents and subsidiaries.
PIPEDA requires online business to obtain
informed consent for the collection, use and disclosure
of individuals» personal information.
Before giving
consent to terminal palliative sedation, a patient who wishes to receive such sedation or, where applicable, the
individual authorized to
consent to care on behalf
of the patient, must among other things be
informed of the prognosis, the irreversible and terminal nature
of the sedation and the anticipated duration
of the sedation.
(iii) An
individual's access to protected health information created or obtained by a covered health care provider in the course
of research that includes treatment may be temporarily suspended for as long as the research is in progress, provided that the
individual has agreed to the denial
of access when
consenting to participate in the research that includes treatment, and the covered health care provider has
informed the
individual that the right
of access will be reinstated upon completion
of the research.
If an
individual revokes a joint
consent, the covered entity that receives the revocation must
inform the other entities covered by the joint
consent of the revocation as soon as practicable.
The following are examples
of valid compound authorizations: an authorization for the disclosure
of information created for clinical research combined with a
consent for the use or disclosure
of other protected health information to carry out treatment, payment, and health care operations, and the
informed consent to participate in the clinical research; an authorization for disclosure
of psychotherapy notes for both treatment and research purposes; and an authorization for the disclosure
of the
individual's demographic information for both marketing and fundraising purposes.
In regard to research projects that include the treatment
of individuals, such as clinical trials, covered entities engaged in these projects will have obtained at least an
informed consent from the
individual to participate in the project.
HHS strongly agrees that IRB review is essential for the adequate protection
of human subjects involved in research, regardless
of whether
informed consent and / or
individuals» authorization is obtained.
(ii) If an
individual revokes a joint
consent, the covered entity that receives the revocation must
inform the other entities covered by the joint
consent of the revocation as soon as practicable.
For this exception to apply, the
individual must have agreed to the denial
of access in conjunction with the
individual's
consent to participate in the research and the covered provider must have
informed the
individual that the right
of access will be reinstated upon completion
of the research.
It is unlikely that a research project that includes the treatment
of individuals could proceed under the Common Rule with a waiver
of informed consent.
Therefore, we require researchers engaged in research projects that include the treatment
of individuals who obtained an IRB waiver
of informed consent under the Common Rule to obtain an authorization or a waiver
of such authorization from an IRB or a privacy board under § 164.512 (i)
of this rule.
Staff are hesitant about giving any form
of evidence — partly as they are busy people, partly as they deal with hundreds
of individuals and recollections may therefore be foggy, but to an extent no doubt from a fear
of being somehow implicated in a negligence action against them or the hospital if they were seen to have treated a patient improperly or without
informed consent.
[236] The central principle is free, prior and
informed consent at all levels: in relation to legal and structural changes and the development
of new policies as well the implementation
of reforms and the involvement
of individuals.
[30] Critically, however, the concepts
of effective participation and prior
informed consent apply not only at a broad level but to
individual events affecting
individual communities:
(a) Document a minimum
of twenty - four hours
of academic preparation or board approved continuing education coursework in counselor supervision training including training six hours in each area as follows: (i) Assessment, evaluation and remediation which includes initial, formative and summative assessment
of supervisee knowledge, skills and self - awareness; components
of evaluation e.g. evaluation criteria and expectations, supervisory procedures, methods for monitoring (both direct and indirect observation) supervisee performance, formal and informal feedback mechanisms, and evaluation processes (both summative and formative), and processes and procedures for remediation
of supervisee skills, knowledge, and personal effectiveness and self - awareness; (ii) Counselor development which includes models
of supervision, learning models, stages
of development and transitions in supervisee / supervisor development, knowledge and skills related to supervision intervention options, awareness
of individual differences and learning styles
of supervisor and supervisee, awareness and acknowledgement
of cultural differences and multicultural competencies needed by supervisors, recognition
of relational dynamics in the supervisory relationship, and awareness
of the developmental process
of the supervisory relationship itself; (iii) Management and administration which includes organizational processes and procedures for recordkeeping, reporting, monitoring
of supervisee's cases, collaboration, research and evaluation; agency or institutional policies and procedures for handling emergencies, case assignment and case management, roles and responsibilities
of supervisors and supervisees, and expectations
of supervisory process within the institution or agency; institutional processes for managing multiple roles
of supervisors, and summative and formative evaluation processes; and (iv) Professional responsibilities which includes ethical and legal issues in supervision includes dual relationships, competence, due process in evaluation,
informed consent, types
of supervisor liability, privileged communication, consultation, etc.; regulatory issues include Ohio laws governing the practice
of counseling and counseling supervision, professional standards and credentialing processes in counseling, reimbursement eligibility and procedures, and related institutional or agency procedures.
Three levels
of consent were sought and obtained: Aboriginal collective
consent at the national level through NACCHO; 24 local community collective
consent from each
individual ACCHS and the Torres Shire Council (representing the Torres Strait community, as there is not a local ACCHS); and
informed consent procured from
individual survey participants by research assistants (5.5)(Box 2).
A thorough research and consultation process, including full information about what a proposal entails (including losses or detriment as well as benefits) in a form that is understood by traditional owner groups, and the right to say no, is necessary to comply with the principle
of free, prior and
informed consent as well as to understand whether changes will support intended outcomes.31 How changing title from communal to
individual ownership through leasing will address other identified impediments to economic development such as inadequate infrastructure in remote areas, under - investment in education and healthcare, high levels
of welfare dependency, high levels
of un-employment and limited job opportunities and limited commercial opportunities is unclear.
Informed consent was obtained from all
individual participants
of 12 years and older included in the study.
73 DOS 95 Matter
of DOS v. Marotta - consolidation
of actions; dual agency; disgorgement
of broker commission; broker may act concurrently in a single transaction as an agent and a principal with
informed consent of and full disclosure to principal; broker's agreement breached by broker where broker obtained property incompatible with client's stated needs; no broker's fee earned where brokerage agreement breached by broker; broker engaging in business under trade name acts as
individual; agency created between broker and buyer by conduct
of parties; dual agency allowed upon full disclosure and
informed consent of both buyer and seller; no commission earned by broker where breach
of fiduciary duty; refund unearned commissions