n. agreement to do something or to allow something to happen only...

The process by which a patient learns about and understands the purpose, benefits, and potential risks of a medical or surgical intervention, including clinical trials, and then agrees to receive the treatment or participate in the trial. Informed consent generally requires the patient or responsible party to sign a statement confirming that they u [..]

A process in which patients are given important information, including possible risks and benefits, about a medical procedure or treatment, a clinical trial, or genetic testing. This is to help them d [..]

Informed consent refers to a person’s agreement to allow personal data to be provided for research and statistical purposes. Agreement is based on full exposure of the facts the person needs to make t [..]

A process used by researchers to communicate with potential and enrolled participants about a clinical study. As part of the informed consent process, researchers: Provide all the important informatio [..]

A duty owed by a medical professional to obtain a patient's consent before performing a procedure or rendering treatment. After fully explaining the treatment, the physician should obtain th [..]

The process through which a person learns about the possible benefits and side effects of a treatment plan and then accepts or declines the treatment. The person is usually asked to sign a consent for [..]

A process during which the patient learns the key facts about HIV testing--including what will occur during HIV testing and counseling and the purpose and benefits of HIV testing--before deciding whet [..]

The voluntary verification of a patient's willingness to participate in a clinical trial, along with the documentation thereof. This verification is requested only after complete, objective information has been given about the trial, including an explanation of the study's objectives, potential benefits, risks and inconveniences, alternat [..]

An agreement to do something or to allow something to happen, made with complete knowledge of all relevant facts, such as the risks involved or any available alternatives. For example, a patient may g [..]

permission from a participant in a user study to participate and to have data collected about them, with that permission hinging on the fact that they have been fully informed of the nature and risks [..]

Permission granted by an individual to use their health information for a specific purpose, with an understanding of what they are agreeing to.

Consent of the patient who has received sufficient information to have surgery, receive medication, or participate in a clinical study.

Participants must give informed consent: voluntary agreement to participate in research by a person or group based on adequate knowledge and understanding of relevant information about the proposed research and what will be expected of participants. These terms may also be used in relation to medical treatment of a patient. Consent may be verbal(sp [..]

consent to medical treatment by a patient or to participation in a medical experiment by a subject after achieving an understanding of what is involved and esp. of the risks

The process in which a patient learns about and understands the purpose and aspects of a clinical trial and then agrees to participate. Of course, a patient may decline to participate. This process includes a document defining how much a patient must know about the potential benefits and risks of therapy before being able to agree to undergo it kno [..]

Person's voluntary agreement, based upon adequate knowledge and understanding, to participate in human subjects research or undergo a medical procedure. In giving informed consent, people may [..]

The agreement between concerned parties about the data-gathering process and/or the disclosure, reporting, and/or use of data, information, and/or results from a research experiment.

Consent to participation in a research study by a participant after achieving an understanding of what is involved. The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision, including details about the study procedures and treatment, the associated risks [..]

Full disclosure of all procedures, requirements, and risks associated with a clinical trial. An informed consent document must be signed before an individual can join a clinical trial.

Informed consent is generally agreement to do something or to allow something to happen only after all the relevant facts are disclosed. Informed consent often refers to consent to a medical procedure [..]

The goal of the informed consent process is to protect participants. It begins when a potential participant first asks for information about a study and continues throughout the study until the study [..]

legally required procedure to ensure that a patient knows about the potential risks and benefits of a treatment before it is started.

Informed consent is a person's voluntary agreement, based on an understanding of the relevant information, to participate in research or a clinical trial, or to undergo a particular medical inter [..]

A process in which an individual is given important facts about a medical procedure, treatment, or clinical trial before deciding whether or not to participate. Informed consent includes information a [..]

is where patients agree to a treatment / randomisation having a reasonable understanding of it.

a  patient's right to know the risks and benefits of a medical procedure.     

(formal notification of) willingness to be a participant in a research study based on an understanding of the nature of the project.

The signed consent of a parent that describes what the parent is consenting to; informed consent must be obtained before a district assesses, makes a major revision to a child’s program, continues, or [..]

signed parental agreement to an action proposed by the district after the parent is provided full information in a way he or she can understand.

Voluntary authorization, by a Patient or Research Subject, with full Comprehension of the Risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.

A communication process between a person and a health care provider or researcher to ensure that the person understands all relevant facts associated with a medical procedure or clinical trial. Before undergoing the procedure or participating in the trial, the person must sign an informed consent form that indicates understanding of the risks and b [..]

Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.

Consent to intervene in a way that is experimental or risky. The participant or guardian is informed of the risks and benefits and of the right to stop the intervention.

Clients (or their advocates) and/or parents and caretakers have the right to be informed about proposed experimental or programmatic outcomes and procedures and their advantages and disadvantages, and [..]

Consent given by a patient after learning about and understanding fully the purpose and other aspects of a clinical trial or procedure.

An ethical requirement that an idividual who gives consent for an invasive medical procedure (e.g. a vaccination) is fully informed of all relevant risks and benefits of the procedure before making th [..]

A process in which a person is given important facts about a medical procedure or treatment, a clinical trial, or genetic testing before deciding whether or not to participate. It also includes informing the patient when there is new information that may affect his or her decision to continue. Informed consent includes information about the possibl [..]

an agreement signed by prospective volunteers for a clinical research trial that indicates their understanding of (1) why the research is being done, (2) what researchers want to accomplish, (3) what [..]

The process of learning the key facts about a clinical trial before deciding whether or not to participate. It is also a continuing process throughout the study to provide information for participants [..]

the process of deciding whether or not to join a clinical trial, after learning enough information to make a responsible decision about participating. All trial participants must provide written agreement before entering a study.

a  process by which a subject voluntarily confirms his or her willingness to participate in a particular trial after having been informed of all aspects of the trial that are relevant to the subject's decision to participate. Informed consent is documented by means of a written, signed and dated informed consent form,

A process by which a subject voluntarily confirms his or her willingness to participate in a particular trial after having been informed of all aspects of the trial relevant to the subject’s decision to participate. Informed consent typically is documented by means of a written, signed and dated informed consent form.

In relation to treatment or proposed treatment, means consent freely given by a person on the basis of information concerning the potential risks and benefits of the treatment that was sufficient information to allow the person to make an informed decision whether to consent to the treatment

a person's legal consent to a medical procedure, such as a vaccination, that is made after the person has been fully informed about the procedure, including its benefits, risks, and alternatives

The process is which a person learns key facts about a clinical trial or research study or medical procedure and then agrees voluntarily to take part or decides against it. This process includes signi [..]

A term used to describe the responsibility of doctors or researchers to ensure that patients or people being researched have an understanding of the relevant facts regarding their care or participation in research. We can also say that consumers have a right to practice informed consent when they buy particular foods. Informed consent relies on our [..]

"Informed consent" means consent given by an individual 15 years of age or older for sterilization that is: (a) Based upon a full understanding of the nature and consequences of sterilizatio [..]

In accordance with 34 Code of Federal Regulations and Education Code: (1) Parent has been fully informed of all information relevant to the activity for which consent is sought, in his/her primary lan [..]

A person's voluntary agreement, based upon adequate knowledge and understanding of relevant information, to participate in research or to undergo a diagnostic, therapeutic, or preventive procedure. It is also a statement of trust between the institution performing the research procedure and the person (eg, a patient) on whom the research proce [..]

Agreement given for something to be done, after the procedure has been fully explained so that the person understands the procedure, possible consequences, and his or her rights to agree or refuse.

Consent means voluntary agreement, or approval to do something in compliance with a request. Informed means that a person’s consent is based on a full disclosure of the facts needed to make the decision intelligently,e.g. knowledge of risks involved, alternatives.

n. agreement to do something or to allow something to happen only after all the relevant facts are known. In contracts, an agreement may be reached only if there has been full disclosure by both parti [..]

Informed consent is a research policy that means participants are made aware of the research and its benefits and implications, and they are given the opportunity to withdraw or move forward.

is considered the standard expression of autonomy of a research participant. Current ethical guidelines insist that researchers who deal with human participants must seek informed consent from participants prior to any research being conducted. The process of obtaining informed consent means that the researcher is required to explain the research p [..]

One of three applications of the basic ethical principles addressed in the Belmont Report (1979), informed consent by research subjects is the moral requirement derived primarily from the ethical principle of respect for persons. Though somewhat controversial, consensus does exist in that informed consent must encompass three critical elements as t [..]

The principle that respondents should know in advance what to expect in a survey or research project and agree to participate based on that knowledge.

Agreement by the participants in an evaluation to the use, in specified ways for stated purposes, of their names and/or confidential information they supplied.

Information exchange between a clinical investigator and research subjects. This exchange may include question/answer sessions, verbal instructions, measures of understanding, and reading and signing informed consent documents and recruitment materials.

A patient giving permission to a physician to carry out a medical procedure after she/he is made fully aware of the benefits, risks, and any alternatives.

Informed consent is consent obtained freely, without coercion, threats or improper inducements, after questions asked by the consumer have been answered, after appropriate disclosure to the patient of [..]

1) Informed consent is a decision to participate in research, taken by a competent individual who has received the necessary information; who has adequately understood the information; and who, after [..]

A person's voluntary agreement, based upon adequate knowledge and understanding of relevant information, to participate in research or to undergo a diagnostic, therapeutic, or preventive procedur [..]

A process of reaching an agreement based on full disclosure. Informed consent has components of disclosure, comprehension, competence and voluntary response. Informed consent often refers to the proce [..]

a procedure whereby information concerning the donation process is presented to the donor or donor’s next of kin with an opportunity for them to ask questions, after which specific approval is documented (AATB Standards 11th edition).

A process of reaching an agreement based on full disclosure. Informed consent has components of disclosure, comprehension, competence and voluntary response. Informed consent often refers to the process by which one decides to donate the organs of a loved one.

Process of giving written permission to have a procedure and indicating that one understands why the procedure is needed, its intended result, and its risks and benefits.

The process requiring a doctor to give a patient enough information about a proposed procedure for the patient to make an informed decision about whether or not to undergo it. The doctor must, in addition to explaining all procedures, address the issues of risks, benefits, alternatives, and potential costs. Infusion

A legal process Receiving and understanding all relevant information, such as potential risks, before agreeing to a medical procedure.

Informed consent is permission given by an individual to proceed with a specific test or procedure, with an understanding of the risks, benefits, limitations, and potential implications of the procedu [..]