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I / I /) CLINICAL TRIAL NOTIFICATION SCHEME Australian Government Department of Health and Aging Therapeutic Goods Administration Notification of Intent to Supply Unapproved Therapeutic Goods under
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FOI 228-1112 document 19 is a specific form or document that is related to the Freedom of Information Act. It is used for reporting certain information or data.
The specific individuals or entities who are required to file FOI 228-1112 document 19 will depend on the regulations and requirements set forth by the governing body or organization. It is important to consult the specific guidelines or instructions provided with the document to determine who must file it.
To fill out FOI 228-1112 document 19, follow the instructions and guidelines provided with the form. Generally, you will need to provide the requested information accurately and completely. It may involve providing personal or organizational details, as well as specific data or reports as specified.
The purpose of FOI 228-1112 document 19 is to collect relevant information or data for certain reporting or regulatory purposes. It serves as a means to gather specific details that are required by the governing body or organization that mandates its filing.
The specific information that must be reported on FOI 228-1112 document 19 will be outlined in the form itself or the accompanying instructions. It typically requires reporting details such as names, dates, financial information, statistical data, or any other relevant information as determined by the governing body or organization.
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