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This advisory outlines the revisions and usage guidelines for the Federal Custody and Control Form (CCF) used in the Federal Workplace Drug Testing Programs, including the extension of the 2000 version
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How to fill out HHS Advisory – Federal Custody and Control Form

01
Obtain the HHS Advisory – Federal Custody and Control Form from the appropriate agency website or office.
02
Begin by filling out the header section with the relevant information such as the date and the case number.
03
Complete the identification section with the details of the subject of the custody and control.
04
Fill in the section specifying the type of federal custody being exercised.
05
Provide detailed descriptions of the items or evidence being controlled, including quantity and condition.
06
Include signatures from the authorized personnel confirming the custody and control.
07
Review the completed form for accuracy before submission.
08
Submit the form to the designated federal agency or department as instructed.

Who needs HHS Advisory – Federal Custody and Control Form?

01
Federal law enforcement agencies.
02
Prosecutors working with federally controlled evidence.
03
Agencies involved in the management of evidence related to federal custody cases.
04
Any other entity requiring documentation of custody and control of federally managed items.
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The HHS Advisory – Federal Custody and Control Form is a document used to ensure proper tracking and accountability of substances regulated by the Department of Health and Human Services (HHS) in federal custody.
Entities or individuals who work with controlled substances, including laboratories, research facilities, and other organizations regulated by HHS, are required to file this form.
To fill out the form, provide required information such as the title of the document, relevant names, contact details, substance information, and signatures where applicable, ensuring all sections are accurately completed.
The purpose of the form is to maintain a clear chain of custody for controlled substances, to comply with regulatory requirements, and to ensure accountability in their handling and transfer.
The information that must be reported includes details about the substances involved, transaction dates, sender and receiver information, quantities, and relevant signatures to certify the transfer.
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