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ID SAMPLE DESTRUCTION AUTHORIZATION From This form is to be used to approve and record the disposal and destruction of biologic samples from clinical trials Name of Trial: Clinical Trial Number: Person
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What is idi sample record destruction?
IDI sample record destruction refers to the process of legally disposing or destroying sample records obtained by an Investigational Device Exemption (IDE) holder during the course of a clinical investigation.
Who is required to file idi sample record destruction?
The IDE holder, who conducted a clinical investigation and obtained the sample records, is required to file the idi sample record destruction.
How to fill out idi sample record destruction?
To fill out idi sample record destruction, the IDE holder should provide the necessary information on the destruction form, including details of the records to be destroyed and the method of destruction. The completed form should then be submitted to the appropriate regulatory authority or governing body.
What is the purpose of idi sample record destruction?
The purpose of idi sample record destruction is to ensure the lawful and secure disposal of sensitive sample records obtained during a clinical investigation, in accordance with regulatory requirements and data protection policies.
What information must be reported on idi sample record destruction?
The idi sample record destruction report should include information such as the date of destruction, a description of the records destroyed, the method of destruction, and any relevant identification numbers or references.
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