Grifols
Formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios.
Grifols fabrica formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios desde sus operaciones de Barcelona. La empresa abastece a canales de farmacias, compradores de hospitales, distribuidores de atención médica o clientes de exportación en sus mercados primarios listados.
- Type
- Manufacturer
- Location
- Barcelona, Spain
- Founded
- 1940
- Website
- grifols.com
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- España, Estados Unidos, Alemania, Brasil
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- fda-registered (green), checked 2026-08-08 FDA
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-08-08 EU EORI validation (European Commission)
- media-mention (green), checked 2026-07-18 Investing.com
- public-subsidy-received (green), checked 2026-08-16 BDNS, Base de Datos Nacional de Subvenciones (Ministerio de Hacienda)
Profiles
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)