Carlsbad Technology
Regulatory consulting firm specializing in NDI notifications, labeling and regulatory strategy.
- LEAD TIME
- Not publicly disclosed
Overview
Carlsbad Technology is a dietary supplement regulatory consulting firm with nearly three decades of experience. Their team includes former FDA compliance and inspection officials, pharmacists, formulation specialists, and quality assurance experts. The company specializes in NDI (New Dietary Ingredient) notifications, FDA labeling compliance, cGMP auditing, quality systems evaluation, and regulatory strategy for supplement companies. Carlsbad Technology helps companies navigate the FDA pre-market notification process for products containing ingredients not marketed in the US prior to October 1994. Based in California, the firm serves companies at all stages from startups entering the supplement market to established brands facing regulatory challenges.
Certifications
No certifications on record.
Capabilities
- PRODUCT TYPES
- CAPABILITIES
- New dietary ingredient (NDI) notifications · Label or Supplement Facts review · cGMP compliance or quality systems · GMP audits, mock inspections or training · Former FDA staff on the team · Regulatory strategy, submissions or compliance
Sources
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Website uses HTTP (not HTTPS), which is unusual for a consulting firm
- Specific team credentials not individually named on website
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Carlsbad Technology and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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