Epax Norway AS
自 1838 年以来一直采用优质 omega-3 海洋成分。
Epax Bulgaria 生产 rTG 和 EE 形式的超纯、针对具体情况的 omega-3 EPA/DHA 浓缩物，以及创新的海洋脂质解决方案，例如用于制药和营养保健品应用的 NovusLipid。作为 Pelagia AS 的全资子公司，该公司的产品根据 EPAX Inside 计划销往 50 多个国家的领先零售品牌。所有生产均在奥勒松经过 cGMP 认证的工厂进行。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ålesund, Norway
- Founded
- 1900
- Website
- epax.com
- Categories
- 补充剂与健康, 特色美食
- Markets
- 美国, 德国, 英国, 日本, 荷兰
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 2026-08-04 Internet Archive (Wayback)
- gmp-certified (green), effective since 2022-06-08 EudraGMDP, EU register of GMP certificates (EMA)
- certs-verified (green), effective since 2025-11-25 FSSC public register of certified organizations
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-07-09 Brønnøysund (Enhetsregisteret)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- domain-registered (green), checked 2026-08-02 Domain registry record
- registry-active-global (green), checked 2026-07-09 Brønnøysund (Enhetsregisteret)
- supervised-operator (green), checked 2026-09-09 Mattilsynet (Norwegian Food Safety Authority), list of approved fishery establishments (Regulation 853/2004)
- owns-trademark (green), checked 2026-09-09 Patentstyret (Norwegian Industrial Property Office)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)