GC Rieber VivoMega
Norwegian producer of EPA and DHA concentrates in ethyl ester and triglyceride forms, plus algal oils.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
GC Rieber VivoMega is a Norwegian omega-3 concentrate manufacturer located in Kristiansund, Norway, with roots dating to GC Rieber's founding in Bergen in 1879. VivoMega produces high-concentration omega-3 EPA and DHA in both ethyl ester and natural triglyceride forms, with total omega-3 content ranging from 70% to 90%. The company invested $75 million in a new state-of-the-art manufacturing facility that opened in May 2024, doubling production capacity. VivoMega also produces certified vegan EPA and DHA algal oils. Their products consistently meet or exceed GOED monograph standards and hold IFOS 5-Star certification. The company maintains a North America sales team.
Certifications
Certification verification in progress. International supplier records require regional database lookups (EudraGMDP, Health Canada NHP, FSSC public register, JHFA directory). See our methodology.
Capabilities
- PRODUCT TYPES
- Omega-3 EPA Concentrates · Omega-3 DHA Concentrates · Triglyceride-Form Omega-3 · Ethyl Ester Omega-3 · Vegan Algal Omega-3 (EPA & DHA)
- CAPABILITIES
- Omega-3s or specialty oils · North American distribution or office
Sources
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Manufacturing in Kristiansund, Norway
- IFOS 5-Star claimed but not independently verified from IFOS consumer reports database
- Omega-3 specialist only. Does not supply other ingredient categories
- $75M facility expansion (May 2024) is recent. Long-term production consistency at the new capacity is not yet established
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between GC Rieber VivoMega and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
Our Evaluation Method
A full assessment applies six checks. Source-Checked listings get a lighter review.
- Independent confirmation: Claims backed by documentation, not marketing copy
- How recent the data is: Information reviewed and dated within the last 12 months
- Sources we traced: Sources cited for every key claim
- Inconsistencies flagged: Where a company's claims and public records disagree, we say so
- What we disclose: Material connections stated directly on affected listings
- What we don't know: When we can't assess something, we say so explicitly
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