Carlsbad Technology
Carlsbad, California
Profile updated: March 26, 2026
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.
Min. Order
Lead Time
Not publicly disclosed
Product Types
Capabilities
NDI Notification Preparation, FDA Labeling Compliance, cGMP Auditing, Quality Systems Evaluation, Regulatory Strategy, Former FDA Officials on Staff
Certifications
Key Regulatory Concepts
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.
Review Notes
Nearly 30 years of dietary supplement regulatory consulting experience. Claims former FDA compliance and inspection officials on staff. NDI notification and cGMP auditing specialization. Website is HTTP-only (unusual for professional services). Specific team credentials not individually named on public website.
Sources
Disclosures
- No material connection exists between Inventory Ready and this company
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