Answer:
D. Increased; decreased
Explanation:
b. price and known dangers
c. specific ingredients and possible side effects
d. manufacturing location and possible side effects
The FDA requires all medication labels to include specific ingredients and possible side effects, to help promote safe usage of medications by providing vital information.
The FDA (Food and Drug Administration) mandates that all medication labels must include c. specific ingredients and possible side effects. This information is crucial for patients and healthcare providers alike, as it details the composition of the drug and the potential harm that it could cause, such as allergic reactions or interactions with other drugs. This requirement aims to promote the safe and effective use of medications by facilitating informed decision-making.
Learn more about FDA regulations here:
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The answer is : all of the above
According to him, organization is a formed when a group of people is gathered together and joined their efforts to achieve a certain goal. The individual purpose and the activities of the members of the organization is irrelevant. As long as that people work with the other members to achieve similar goal, their presence could be considered as an organization.
Answer:
Harsh sanctions work as an effective deterrence to recidivism.
Explanation:
To explain this option, lets first define recidivism. Recidivism is simply defined as the tendency of a criminal who has been convicted before to re-offend. One thing about crime and harsh sanctions is that, harsh sanctions does not stop a victim from re-offending. There is every tendency that an offender with a lighter sanction will not re-offend, and one with a harsh sanction will continue to re-offend. It is based on many factors such as ways of upbringing, exposure to drug use and other crimes etc.
b. To obtain a signature from a study subject in order to protect the investigator, the study staff and the institution.
c. To document the investigator's participation in the consent process.
d. To obtain a signature from a study subject in order to document his or her agreement to participate in research.
The purpose of informed consent in medical research is to provide potential subjects with the necessary information so they can make an informed decision about participation. It is not about protecting the investigator or institution, but rather respecting the autonomy and rights of the subject.
The purpose of informed consent in medical research is to provide potential subjects with appropriate information in an appropriate manner, enabling them to make an informed decision about participating in research. It involves ensuring that the subject understands the nature of the study, risks and benefits, procedures involved, and any alternatives. Informed consent is not about obtaining a signature to protect the investigator or institution but rather about respecting the autonomy and rights of the subject.
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Informed consent in research primarily aims to provide potential participants with appropriate and complete information about the study, enabling them to make an informed decision about their participation. Signatures are used for documentation, but the key purpose is ensuring the participant's understanding and choice.
The purpose of informed consent in research is mainly to provide a potential participant with all the necessary information about the study, and allow that person to make an informed decision about their participation. That's why option 'a' is the correct one. While obtaining a signature does indeed document an individual's agreement to participate, the core of informed consent is rooted in the ethics of research and stresses the importance of clarity, understanding, and freedom of choice for the participant. The options 'b', 'c', and 'd' are parts of the consent process, but none of them fully capture the primary purpose of informed consent.
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