PRODITEC SAS
1987 yılında kurulan Proditec, ilaç ve darphane endüstrilerine yönelik otomatik görsel denetim çözümlerinin lider üreticisidir. Avrupa
1987 yılında kurulan Proditec, ilaç ve darphane endüstrilerine yönelik otomatik görsel denetim çözümlerinin lider üreticisidir. Avrupa, Asya ve Kuzey Amerika'da 3 ofisi bulunan ve
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Pessac, France
- Founded
- 1987
- Website
- proditec.com
- Categories
- İlaç Üretimi
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-20 Domain registry record
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-09-03 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- debarment-clear (green), checked 2026-07-30 OpenSanctions
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-07-30 OpenSanctions
- registry-active-global (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- vat-valid (green), checked 2026-07-30 VIES
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)