Investigational drugs

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Actual: Disposition of unused supply of investigational drug. 312.60: General responsibilities of investigators. 312.61: Control of the investigational drug. 312.62: Investigator recordkeeping and record retention. 312.64: Investigator reports. 312.66: Assurance of IRB review. 312.68: Inspection of investigator's records and reports
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An Investigational New Drug Application (IND) is a request for authorization from the Food and Drug Administration (FDA) to administer an investigational drug

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Investigational new drug (IND) means a new drug or biological drug that is used in a clinical investigation.

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For investigational drugs, contact or . For investigational biologics, contact

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streetdrugs investigation undercover This section covers investigative techniques of drug investigation. The following topics are

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Investigational Drugs and Devices (IND/IDE) As defined by the Food and Drug Administration (FDA), an IND, or investigational new drug application, is a request for authorization from the FDA to administer an investigational drug or biological product to humans.

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Regulation on Approval for Investigational New Drug Application of Drugs.(No. , ) Regulation on Approval for Investigational New Drug Application of

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an investigational drug for use under the IND ( 312.8(a)). Often the manufacturer of the investigational drug is the sponsor of the IND under which clinical studies of the investigational

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Fast Track Designation facilitates the development of investigational drugs and allows for expedited review Investigational New Drug

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An experimental drug may be approved by the FDA for use in one disease or condition but still be considered investigational in other diseases or conditions. Also called IND, investigational agent, investigational drug, and investigational new drug.

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