GRASroots Consulting
GRASroots Consulting is a regulatory consulting firm focused on US food and dietary supplement ingredient safety and market access. The firm prepares feasibility and gap assessments, independent Generally Recognized as Safe (GRAS) conclusions, FDA GRAS Notices (GRNs), and New Dietary Ingredient (NDI) notifications, and supports FDA pre-notification meetings. GRASroots has appeared as the notifying agent on a GRAS notice in FDA's public GRAS Notice docket. The firm states it has provided science-based GRAS and NDI support since 2006.
Enumclaw, Washington
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
GRASroots Consulting is a regulatory consulting firm focused on US food and dietary supplement ingredient safety and market access. The firm prepares feasibility and gap assessments, independent Generally Recognized as Safe (GRAS) conclusions, FDA GRAS Notices (GRNs), and New Dietary Ingredient (NDI) notifications, and supports FDA pre-notification meetings. GRASroots has appeared as the notifying agent on a GRAS notice in FDA's public GRAS Notice docket. The firm states it has provided science-based GRAS and NDI support since 2006.
§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
- GRAS Conclusions · FDA GRAS Notices · NDI Notifications · Feasibility and Gap Assessments · Regulatory Strategy
- CAPABILITIES
- Independent GRAS conclusions · FDA GRAS Notices (GRNs) · New Dietary Ingredient (NDI) notifications · Feasibility and gap assessments · FDA pre-notification meeting support · Science-based safety and risk evaluations
§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 GRASroots Consulting and other vendors, capabilities, and certifications is in the manufacturer atlas.
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