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ANNEX 1: Application Form for Registration of Human Medicinal Product (Quality Information Summary) F01/FDA/DMC/MCE/G/001 Rev. No. 4 APPLICATION FORM FOR REGISTRATION OF HUMAN MEDICINAL PRODUCT (QUALITY
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Start by carefully reading the instructions provided on the form or any accompanying guidance material. This will help you understand the purpose of the form and the information it requires.
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The annex 1 application form is a form that contains specific information required for a particular process or application.
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