Freyr Dietary Supplement Regulatory Services
Freyr is a global regulatory-affairs services firm with a dedicated dietary supplement and food-supplement practice supporting US FDA compliance. Services include facility registration support, New Dietary Ingredient (NDI) and GRAS notification support, labeling and claims review and substantiation, ingredient and formulation review, and regulatory submissions. Freyr was recognized as a Leader in the Everest Group Life Sciences Regulatory and Medical Affairs Operations PEAK Matrix assessment for 2024. The firm reports a large regulatory team operating across many countries.
Not disclosed
Directory Listing · Records Reviewed
Public records and independent sources have been reviewed.
What this means →- MOQMOQ (Minimum Order Quantity)The smallest production run a manufacturer will accept for an order.
- Not publicly disclosed
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
Freyr is a global regulatory-affairs services firm with a dedicated dietary supplement and food-supplement practice supporting US FDA compliance. Services include facility registration support, New Dietary Ingredient (NDI) and GRAS notification support, labeling and claims review and substantiation, ingredient and formulation review, and regulatory submissions. Freyr was recognized as a Leader in the Everest Group Life Sciences Regulatory and Medical Affairs Operations PEAK Matrix assessment for 2024. The firm reports a large regulatory team operating across many countries.
§2Our review
The six checks in our review, applied before any name appears in the directory. Each check is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
No certifications on record.
§5Capability matrix
- PRODUCT TYPES
- NDI and GRAS Support · Facility Registration Support · Labeling and Claims Compliance · Ingredient and Formulation Review · Regulatory Submissions
- CAPABILITIES
- Dietary supplement facility registration support · New Dietary Ingredient (NDI) and GRAS notification support · Labeling and claims review and substantiation · Ingredient and formulation regulatory review · FDA regulatory submissions and liaison
§6Sources
Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.
Disclosures
- No material connection exists between Inventory Ready and this company
For the check-by-check breakdown that produces this vendor's score, see our scoring framework. The connection map between Freyr Dietary Supplement Regulatory Services and other vendors, capabilities, and certifications is in the manufacturer atlas.
Interested in Freyr Dietary Supplement Regulatory Services?
Tell us about your project and we'll help you determine if this regulatory consultant is a good fit.