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The Italian Medicines Agency
Organization
Committees
Observatories
Communication
Activities
Clinical Trials
Assessment and registration
Post-Marketing Surveillance
Inspections and Certification
Pharmaceutical Policy
Pricing and Reimbursement
Medical and Scientific Information
The independent research on drugs
International Relations
Counterfeit medicines
Quick links menu
AIFA Front End
AIFA Check Point – Variation Type I (How to submit a Variation Type I online)
Fees
SIS Codes
Authorization for congresses and meetings
National Monitoring Centre for Clinical Trials
Reporting an adverse drug reaction
Report Clinical Trials of Drugs in Italy 2011
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