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Investigational Medicinal Product Destruction Log Site Name:___ PI:___Trial Name: ___ Extract No.:___Investigational medication product should not be destroyed without prior written authorization
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How to fill out investigational product destruction form

01
Obtain a copy of the investigational product destruction form from your institution or the appropriate regulatory body.
02
Fill in the basic details such as the date of destruction, name of the investigator, and name of the sponsor.
03
Provide information about the investigational product being destroyed, including the name, batch numbers, and quantity.
04
Indicate the reason for the destruction and any supporting documentation that may be required.
05
Include details about any witnesses present during the destruction process.
06
Sign and date the form to acknowledge that the destruction has been completed.
07
Submit the completed form to the relevant authority or keep it on file for future reference.

Who needs investigational product destruction form?

01
Investigators conducting clinical trials
02
Institutional review boards (IRBs)
03
Ethics committees
04
Regulatory bodies

What is INVESTIGATIONAL PRODUCT DESTRUCTION J Form?

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The investigational product destruction form is a document used to formally record the destruction of investigational products that are no longer needed or are being disposed of for safety reasons.
The entity responsible for the management of the investigational product, such as a clinical trial sponsor or investigator, is required to file the investigational product destruction form.
To fill out the investigational product destruction form, you need to provide details such as the product name, quantity being destroyed, reason for destruction, the date of destruction, and signatures of responsible parties.
The purpose of the investigational product destruction form is to ensure accountability and traceability of investigational products that are no longer in use, thus avoiding potential misuse or safety issues.
The form must report information such as the investigational product details, amount destroyed, batch number, destruction date, and signatures of the individuals responsible for the destruction.
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