Procaps
Capsules molles, médicaments, suppléments et produits pharmaceutiques.
Procaps fabrique des gélules molles, des médicaments, des suppléments et des produits pharmaceutiques à partir de ses opérations de Barranquilla. L'entreprise fournit des pharmacies, des acheteurs de soins de santé, des équipes de marchés publics ou des clients exportateurs sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Barranquilla, Colombia
- Founded
- 1977
- Website
- procaps.com
- Categories
- Fournitures médicales et de santé, Compléments et bien-être
- Markets
- Colombie, Pérou, États-Unis, Mexique
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- lei-lapsed (amber), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-08-16 RUES, Registro Único Empresarial y Social (Confecámaras)
- registered-since (green), checked 2026-08-16 RUES, Registro Único Empresarial y Social (Confecámaras)
- leadership-on-record (green), checked 2026-08-16 RUES, Registro Único Empresarial y Social (Confecámaras)
- registry-activity (green), checked 2026-08-16 RUES, Registro Único Empresarial y Social (Confecámaras)
- registered-units (green), checked 2026-08-16 RUES, Registro Único Empresarial y Social (Confecámaras)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)