REGULATORY COMPLIANCE
Registrar Corp
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.
Hampton, Virginia
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.
- Service-based (per registration or review)
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
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.
§2Six-gate readout
Six gates we apply before any name appears in the directory. Each gate is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
No certifications on record.
§5Capability matrix
- PRODUCT TYPES
- FDA Registration · Label Review · MMR Review · Prior Notice · Adverse Event Reporting
- CAPABILITIES
- FDA Facility Registration & Renewal · Label & Ingredient Compliance Review · Master Manufacturing Records Review · Prior Notice Submission · Adverse Event Report Forwarding · US Agent Representation · Detention Assistance · MyFDA Compliance Platform
§6Sources
- Registrar Corp Official Website(2026-03-13)
- Registrar Corp Dietary Supplements(2026-03-13)
- Registrar Corp Compliance Services(2026-03-13)
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
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