AIBMR Life Sciences
AIBMR Life Sciences, Inc. is an independent scientific and regulatory consulting firm founded in 1978, serving the dietary supplement, food, and natural products industries. The firm prepares GRAS (Generally Recognized as Safe) independent conclusions and FDA GRAS notifications, New Dietary Ingredient (NDI) notifications, and toxicology and safety assessments, and coordinates expert safety panels. AIBMR has been named as the notifying agent on FDA GRAS notices for dietary ingredients and maintains a public database of independent GRAS conclusions.
Puyallup, 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
AIBMR Life Sciences, Inc. is an independent scientific and regulatory consulting firm founded in 1978, serving the dietary supplement, food, and natural products industries. The firm prepares GRAS (Generally Recognized as Safe) independent conclusions and FDA GRAS notifications, New Dietary Ingredient (NDI) notifications, and toxicology and safety assessments, and coordinates expert safety panels. AIBMR has been named as the notifying agent on FDA GRAS notices for dietary ingredients and maintains a public database of independent GRAS conclusions.
§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 Independent Conclusions · FDA GRAS Notifications · NDI Notifications · Toxicology and Safety Assessment · Regulatory Compliance
- CAPABILITIES
- GRAS self-determination and FDA GRAS notification preparation · New Dietary Ingredient (NDI) notifications · Toxicology and safety assessment · Expert safety panel coordination · FDA and FTC regulatory compliance
§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 AIBMR Life Sciences and other vendors, capabilities, and certifications is in the manufacturer atlas.
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