• Register company and facilities with ANMAT.

• Obtain GS1 identifiers and configure serialization capability.

• Serialize each pack during packaging.

• Report commissioning data to the ANMAT database.

• Report distribution events when product moves between supply chain actors.

• Report dispensing events when supplied to the patient.

• Submit return and decommission events where applicable.

All traceability data must be reported to the ANMAT National Medicines Traceability System (SNT).

Key characteristics:

• Central government database

• Real time event monitoring

• API based reporting

• Web portal available for manual reporting

The system allows regulators to monitor each medicine from manufacturing through dispensing to patients. (Argentina)

Participants must register their facilities and identifiers such as:

GLN (Global Location Number) from GS1
CUFE (physical establishment code assigned by ANMAT)

• Aggregation is not mandatory in the Argentina system.
• However:
  
  • Many companies implement case and pallet aggregation internally to simplify logistics and reporting.
  • Serial level reporting remains mandatory regardless of aggregation.
• The system tracks products primarily through individual serialized units rather than SSCC hierarchies.

• Incorrect GTIN configuration for registered products.

• Failure to report distribution or receipt events between supply chain partners.

• Mismatch between printed serial numbers and reported data.

• Using unregistered facility identifiers in traceability reports.

• Late reporting of dispensing events by pharmacies.