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Federal Agency for Medicines and Health Products Avenue Galilee Galilean 5/03 1210 BRUSSELS www.fagg.be www.afmps.be DirectorateGeneral PRE authorization Research and Development Division (human use)Guideline
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Read the guidelines carefully to understand the submission requirements.
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Prepare all necessary documents and information requested in the guidelines.
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Fill out the submission form accurately and completely.
04
Review the submission for any errors or missing information.
05
Submit the completed form according to the specified method in the guidelines.

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Companies or individuals who are required to submit proposals, applications, or requests for approval to a governing body or organization.
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Guideline submission processes involve submitting guidelines or protocols for review and approval.
Any individual or organization who wishes to have their guidelines reviewed and approved must file guideline submission processes.
Guideline submission processes can typically be filled out online or by submitting physical forms to the relevant authority.
The purpose of guideline submission processes is to ensure that guidelines are reviewed, approved, and implemented correctly.
Information such as the purpose of the guidelines, methodology used, and potential impact on stakeholders must be reported on guideline submission processes.
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