Diaco Biofarmaceutici Srl

Listed in a source registry

PharmaSource directory

Verified facts

• state-aid-sector (green), checked 2026-04-28 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
• registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
• lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
• operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
• export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
• vat-valid (green), checked 2026-08-01 VIES (European Commission)

Profiles

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Import rules for these goods

• Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)

Check independently

• Sanctions and watchlists (OpenSanctions)
• VAT number check (EU VIES)