Registrar Corp
Provider of label and ingredient review, master manufacturing record review and prior notice submissions.
- ENGAGEMENT
- Per registration or review
- LEAD TIME
- Not publicly disclosed
Overview
Registrar Corp is an FDA compliance solutions provider serving over 30,000 food, beverage, dietary supplement, drug, medical device, and cosmetic companies worldwide. Based in Hampton, Virginia, the company specializes in FDA facility registration, label and ingredient review, Master Manufacturing Records (MMR) review, Prior Notice submissions, and adverse event reporting. Registrar Corp's MyFDA platform provides ongoing compliance management tools. Their regulatory specialists review product labels against FDA requirements and provide detailed reports with recommended changes and ready-to-use compliant label graphic files.
Certifications
No certifications on record.
Capabilities
- PRODUCT TYPES
- FDA Registration · Label Review · MMR Review · Prior Notice · Adverse Event Reporting
- CAPABILITIES
- Label or Supplement Facts review · Formula or ingredient compliance review · cGMP compliance or quality systems · FDA inspection, 483, warning-letter or detention response · FDA registration, US Agent or Prior Notice · Adverse event reporting
Sources
- Registrar Corp Official Website(2026-03-13)
- Registrar Corp Dietary Supplements(2026-03-13)
- Registrar Corp Compliance Services(2026-03-13)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Compliance services provider, not a hands-on regulatory strategist; best for registration and label compliance tasks
- No third-party certifications or accreditations found for the company itself
- Pricing not publicly disclosed
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Registrar Corp 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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