MILÉNICA HEALTHCARE S.L.
在 Milénica Healthcare,我们专注于制药行业和医疗保健行业的国际贸易
在 Milénica Healthcare,我们专注于制药行业和医疗保健行业的国际贸易。 我们提供广泛的药品、医疗产品和膳食补充剂目录,以及旨在支持医疗保健行业内公司(供应商和分销商)的运营和战略活动的一系列服务。 感谢我们的团队、联系网络和合作者,我们可以提供在欧洲、中东、拉丁美洲、非洲和亚洲进出口所需的所有必要结构和信息。 我们的目的是
- Type
- Distributor
- Location
- Madrid, Spain
- Website
- milenicahealthcare.com
- Categories
- 药品制造, 医疗保健用品, 补充剂与健康
- Markets
- 西班牙
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-09 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 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)