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INSTRUCTIONS FOR REPORTING OF LOCAL and NONVOCAL ADVERSE EVENTSDEFINITIONSA. Investigational Product: Any drug, biologic, radio pharmaceutical, vaccine, natural health product, medical device or placebo
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Who needs investigational product any drug?

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Individuals who are participating in a clinical trial or research study may need to use investigational product any drug.
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These individuals are usually under the supervision of healthcare professionals and are closely monitored during the course of the study.
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Investigational products are often used in experimental therapies or treatments that have not yet been approved by regulatory authorities for general use.
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Therefore, individuals who have exhausted other treatment options or have specific medical conditions that require alternative interventions may also be candidates for investigational products.
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It is important to note that the use of investigational products should be done in compliance with ethical guidelines and under the guidance of healthcare professionals.

What is Investigational Product: Any drug, biologic, radiopharmaceutical, vaccine, natural health product, medical device or placebo being given to a research participant Form?

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An investigational product is any drug that is being studied in a clinical trial.
The sponsor of the clinical trial is required to file the investigational product.
The investigational product can be filled out by providing all relevant information about the drug being studied in the clinical trial.
The purpose of an investigational product is to gather data on the safety and effectiveness of the drug being studied.
The information that must be reported includes the name of the drug, the dosage, any adverse reactions, and the results of the clinical trial.
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