MILÉNICA HEALTHCARE S.L.
At Milénica Healthcare, we specialize in international trade for the pharmaceutical industry and the healthcare sector
At Milénica Healthcare, we specialize in international trade for the pharmaceutical industry and the healthcare sector. We offer a wide catalog of medications, medical products, and dietary supplements, along with a range of services designed to support the operations and strategic activities of companies (both suppliers and distributors) within the healthcare sector. Thanks to our team, our network of contacts and collaborators, we provide access to all the necessary structure and information to import and/or export in Europe, the Middle East, Latin America, Africa, and Asia. Our purpose i
- Type
- Distributor
- Location
- Madrid, Spain
- Website
- milenicahealthcare.com
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Supplements & Wellness
- Markets
- Spain
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
Profiles
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
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)
- 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)