Laboratorio Pablo Cassará
Entreprise pharmaceutique et biotechnologique argentine produisant des injectables génériques, des produits biologiques oncologiques…
Société pharmaceutique et biotechnologique argentine produisant des injectables génériques, des produits biologiques oncologiques et des biosimilaires ; collaborer avec le gouvernement argentin pour la fabrication locale de remplissage et de finition du vaccin COVID.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Buenos Aires, Argentina
- Founded
- 1937
- Website
- cassara.com.ar
- Categories
- Fournitures médicales et de santé
- Markets
- Argentine, Brésil, Chili, Mexique
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
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- domain-registered (green), checked 2026-08-02 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)