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Children in clinical research and Clinical trial

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Children in clinical research and Clinical trial

Children in clinical research vs. Clinical trial

In health care, a clinical trial is a comparison test of a medication or other medical treatment (such as a medical device), versus a placebo (inactive look-alike), other medications or devices, or the standard medical treatment for a patient's condition. Clinical trials are experiments or observations done in clinical research.

Similarities between Children in clinical research and Clinical trial

Children in clinical research and Clinical trial have 9 things in common (in Unionpedia): Declaration of Helsinki, Food and Drug Administration, Informed consent, Institutional review board, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, Medical device, Medication, National Institutes of Health, Placebo.

Declaration of Helsinki

The Declaration of Helsinki (DoH) is a set of ethical principles regarding human experimentation developed for the medical community by the World Medical Association (WMA).

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Food and Drug Administration

The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.

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Informed consent

Informed consent is a process for getting permission before conducting a healthcare intervention on a person, or for disclosing personal information.

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Institutional review board

An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a type of committee that applies research ethics by reviewing the methods proposed for research to ensure that they are ethical.

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International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is a project that brings together the regulatory authorities of Europe, Japan and the United States and experts from the pharmaceutical industry in the three regions to discuss scientific and technical aspects of pharmaceutical product registration.

Children in clinical research and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use · Clinical trial and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use · See more »

Medical device

A medical device is any apparatus, appliance, software, material, or other article—whether used alone or in combination, including the software intended by its manufacturer to be used specifically for diagnostic and/or therapeutic purposes and necessary for its proper application—intended by the manufacturer to be used for human beings for the purpose of.

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Medication

A medication (also referred to as medicine, pharmaceutical drug, or simply drug) is a drug used to diagnose, cure, treat, or prevent disease.

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National Institutes of Health

The National Institutes of Health (NIH) is the primary agency of the United States government responsible for biomedical and public health research, founded in the late 1870s.

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Placebo

A placebo is a substance or treatment of no intended therapeutic value.

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The list above answers the following questions

Children in clinical research and Clinical trial Comparison

Children in clinical research has 27 relations, while Clinical trial has 178. As they have in common 9, the Jaccard index is 4.39% = 9 / (27 + 178).

References

This article shows the relationship between Children in clinical research and Clinical trial. To access each article from which the information was extracted, please visit:

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