Spherix Consulting Group
Spherix Consulting Group is a scientific and regulatory consulting firm supporting food and dietary supplement companies with FDA regulatory submissions. Services include New Dietary Ingredient (NDI) notifications, Generally Recognized as Safe (GRAS) determinations, food additive petitions, and regulatory strategy. The Council for Responsible Nutrition has featured a Spherix senior project manager discussing dietary supplement regulatory topics. Spherix is based in Rockville, Maryland and describes itself as a global team serving food, supplement, consumer-product, and pharmaceutical clients.
Rockville, Maryland
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
Spherix Consulting Group is a scientific and regulatory consulting firm supporting food and dietary supplement companies with FDA regulatory submissions. Services include New Dietary Ingredient (NDI) notifications, Generally Recognized as Safe (GRAS) determinations, food additive petitions, and regulatory strategy. The Council for Responsible Nutrition has featured a Spherix senior project manager discussing dietary supplement regulatory topics. Spherix is based in Rockville, Maryland and describes itself as a global team serving food, supplement, consumer-product, and pharmaceutical clients.
§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 Notifications · GRAS Determinations · Food Additive Petitions · FDA Regulatory Submissions · Regulatory Strategy
- CAPABILITIES
- New Dietary Ingredient (NDI) notifications · GRAS determinations · Food additive petitions · FDA regulatory submissions · Dietary supplement regulatory strategy
§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 Spherix Consulting Group and other vendors, capabilities, and certifications is in the manufacturer atlas.
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