FORMULATION RD
Nutralliance
Nutralliance is a dietary supplement R&D and formulation consultancy based in Irvine, California. The company provides formulation services, ingredient sourcing, regulatory guidance, and product development support for supplement brands. Unlike full-service CMOs, Nutralliance focuses on the front-end product development phase; helping brands design formulas, select ingredients, navigate regulatory requirements, and prepare products for manufacturing. They also offer stability study coordination and clinical trial design assistance.
Irvine, California
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.
- Project-based (consulting)
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
Nutralliance is a dietary supplement R&D and formulation consultancy based in Irvine, California. The company provides formulation services, ingredient sourcing, regulatory guidance, and product development support for supplement brands. Unlike full-service CMOs, Nutralliance focuses on the front-end product development phase; helping brands design formulas, select ingredients, navigate regulatory requirements, and prepare products for manufacturing. They also offer stability study coordination and clinical trial design assistance.
§2Six-gate readout
Six gates we apply before any name appears in the directory. Each gate is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
0 of 1 certification independently confirmed. What this means
§5Capability matrix
- PRODUCT TYPES
- Formulation Consulting · Capsules · Tablets · Powders · Softgels · Beverages
- CAPABILITIES
- Custom Formulation Development · Ingredient Sourcing · Regulatory Consulting · Stability Study Coordination · Clinical Trial Design · New Product Launch Support
- DOSAGE FORMS
- capsules · powders · softgels · tablets
§6Sources
- Nutralliance Official Website(2026-03-13)
- Nutralliance Services(2026-03-13)
- Nutralliance LinkedIn(2026-03-13)
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.
What We Couldn't Verify
- Formulation consultancy, not a manufacturer; does not produce finished products
- No manufacturing-related certifications (NSF GMP, etc.) as they do not manufacture
- Primarily a service/consulting company; limited public information available compared to manufacturers
- On-site facility inspection was not conducted
Last reviewed: March 13, 2026
Disclosures
- No material connection exists between Inventory Ready and this company
Our Evaluation Method
Every manufacturer assessment follows six principles:
- Evidence: Claims backed by documentation, not marketing copy
- Freshness: Information reviewed and dated within the last 12 months
- Provenance: Sources cited for every key claim
- Challenge: Inconsistencies flagged, not hidden
- Disclosure: Material connections stated directly on affected listings
- Abstention: When we can't assess, we say so explicitly
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