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Registrar

Registrar

Assistance with U.S. FDA Regulations

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FDA Compliance Monitor

Automate Supply Chain Risk Management

Easily identify vulnerabilities in your supply chain using the FDA Compliance Monitor.

Registrar Corp assists businesses with U.S. FDA compliance.

Registrar Corp is not affiliated with the U.S. FDA

Learn More

Cost-effective compliance is only a few clicks away

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  • Provide your company information

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  • Food Safety

    Is your Food Safety Plan FDA-Compliant?

    U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.

  • Food Safety

    U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.

  • Food Label Deadline

    Deadline Approaching for FDA's New Label Rules

    Many food companies have less than 12 months to update their labeling to comply with new FDA labeling rules. The new rules include updates to the nutrition facts chart, serving sizes, mandatory declarations, and more.

  • Food Label Deadline

    Labeling mistakes result in more than 22% of all detentions in the United States.

    Many companies do not realize their labels are non-compliant until their products are detained, which may result in delays, re-labeling expenses, or destruction of inventory. Help avoid costly issues in port. Have Registrar Corp's experts assess the FDA compliance of your labels.

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      • NOTE: Registrar Corp cannot verify or recover your registration without:

        • Your Registration Number and PIN
        • or
        • your FURLS Login and Password.

        If you do not have either set of information, we encourage you to re-register.

        Re-Register Now
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      • (11 Digit Number)
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      • Compliance Information

      •  
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                    • Provide the following information for each of your NIOSH approved respirators
                      Manufacturer NameModel NumberNIOSH Approval Number 
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                      • Issued by another regulatory authority or conformity assessment body. Include the authorization number and name of the assessment body (if applicable)
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                          • Report should demonstrate applicable performance standards have been met
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                            FSMA Made Easy

                            Supplier monitoring deadlines have passed. Simplify compliance using the FDA Compliance Monitor.

                            Get Started

                            Registrar Corp assists businesses with U.S. FDA compliance.

                            Registrar Corp is not affiliated with the U.S. FDA

                            Meet The FDA Compliance Monitor

                            Know Sooner. Act Faster. Reduce Risk.

                            Now you can track your suppliers’ compliance, gauge your suppliers’ risk, and manage your suppliers’ documentation from one simple and secure platform.

                            Supply-Chain Management

                            Track and approve your suppliers in one centralized interface.

                            Automated Supplier Checks

                            Get current information on your suppliers, aggregated from six FDA databases.

                            Email Alerts

                            Receive immediate alerts when a supplier’s compliance changes.

                            Top Notch Security

                            Protect your data by managing supplier compliance in a highly secure environment.

                            Continuously Monitor Suppliers For:

                            FDA Registration Numbers

                            FDA Inspection Classifications

                            Import Alerts

                            Warning Letters

                            Import Refusals

                            Recalls

                            Customer Testimonials

                            Using the Monitor is by far the best tool for FSVP monitoring. This is especially true when you consider the speed, cost, and accuracy when compared to staffing someone in-house.

                            – Jamie Jones

                            Director of European Operations | La Tienda

                            The FDA Compliance Monitor tool is a great product that allows us to quickly and effectively evaluate current and potential suppliers. The Registrar Corp team has been an invaluable resource for all our FDA related inquiries.

                            – Stephanie Billings

                            Regulatory Compliance Manager | TJX Companies

                            The FDA Compliance Monitor was invaluable during our SQF Audit.  We were able to display our supply chain and show auditors the level of our due dilligence on our suppliers. Auditors were impressed and we passed our audit.

                            – Emma Raven

                            Quality Compliance Manager | Capstone Nutrition

                            We were looking at a great deal of time and money needing to be spent to manually research and track over 150 suppliers in our importing business. After investigating several options, we felt that FDA Monitor from Registrar Corp was the perfect solution for our situation. The company understands the subtleties of the importing business, and the complexities of working with international suppliers in multiple countries.

                            – Steve Brunsting

                            Vendor Compliance & Sourcing Manager | Limson Trading Inc.

                            A top feature is the ability to link the document system with the existing multi-supplier monitoring. Another important feature of the DMS is the rapid response of Registrar Corp’s development team that allows for customization and constant improvement. The customer service response times to our suggestions have been excellent.

                            – Frederick Robinson

                            Director of R&D and Co-pack Quality | Jasper Wyman & Son

                            Dive Deeper into Compliance with

                            A powerful scoring system that helps evaluate the risk your suppliers may present based on their FDA compliance and shipment history.

                            RegiScore
                            93
                            Low Risk

                            Evaluate supplier risk using a score of 0 to 100

                            144 Cleared Shipments
                            HIGH IMPACT
                            1 VAI Inspection
                            LOW IMPACT

                            View factors that impact a supplier’s score

                            87
                            CIDER VINEGAR
                            54
                            CONDIMENTS, N.E.C.
                            76
                            ITALIAN DRESSING

                            Assess the risk of your supplier’s individual products

                            Enhance your monitoring with the Document Management System (DMS)

                            Maintain Required Recordkeeping and Supplier Documentation

                            Easily manage any document you need

                            Manage Food Safety Plans, inspection reports, process documentation, and more by leveraging Registrar Corp’s robust library of templated documents.  Alternatively, you can create your own document types with custom attachments and validity periods.

                            Request, evaluate, and approve documentation

                            Upload compliance documents you have on file or request records directly from your suppliers.  A dynamic versioning feature allows you to maintain a document over several years with records of its validity and approval status.

                            Receive automated actionable notifications

                            The Monitor’s notification system sends alerts when documents are ready to review and when they need to be re-assessed.  Easily maintain compliance with recordkeeping requirements in spite of challenges, such as tracking document validity and staffing changes.

                            Transform Your Supplier Discovery with Marketplace

                            • Source global suppliers with proven track records of consistent FDA compliance on a single platform.

                            • Narrow potential suppliers by factors such as RegiScore, shipment volume and frequency, or exporting country.

                            • Add potential suppliers to your account to continuously monitor their FDA compliance and manage their documentation.

                            Learn More

                            Cost-Effective Compliance

                            Start monitoring today for as little as $58 a month.

                            See how much you can save
                            • Monitor + DMS
                            • Monitor Only

                            5 Facilities

                            $83/month

                            • $16.60/month per facility
                            • 8% Savings

                            25 Facilities

                            $388/month

                            • $15.50/month per facility
                            • 6% Savings

                            50 Facilities

                            $761/month

                            MOST POPULAR!

                            • $15.22/month per facility
                            • 8% Savings

                            51+ Facilities

                            Custom Pricing

                            • Reach out for a custom plan

                            5 Facilities

                            $58/month

                            • $11.60/month per facility
                            • 8% Savings

                            25 Facilities

                            $265/month

                            • $10.60/month per facility
                            • 9% Savings

                            50 Facilities

                            $516/month

                            MOST POPULAR!

                            • $10.32/month per facility
                            • 11% Savings

                            51+ Facilities

                            Custom Pricing

                            • Reach out for a custom plan

                            Not seeing the right plan for your business?

                            Proactive Compliance Using Actionable Data

                            Streamline supply chain management today.

                            • Features
                            • Track supplier compliance
                            • Gauge supplier risk
                            • Manage supplier documents
                            • Source compliant suppliers

                            Solutions

                            Enregistrement FDA

                            FDA Compliance Monitor

                            Etiquetage FDA

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                            Téléphone: +1-757-224-0177

                            Fax: +1-757-224-0179

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                            © 2025 Registrar Corp

                            144 Research Drive Hampton, Virginia 23666 USA
                            Conditions d'utilisation | Politique de confidentialité

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                            Attention: les établissements qui n’auront pas renouvelé leur enregistrement FDA en   devront se réenregistrer

                            Attention: les établissements pharmaceutiques et de dispositifs médicaux qui n’auront pas renouvelé leur enregistrement FDA en   devront se réenregistrer.

                            Se réenregistrer maintenant

                            Les établissements enregistrés à la FDA doivent renouveler leurs enregistrements avant le 31 décembre  

                            Les établissements pharmaceutiques et de dispositifs médicaux enregistrés à la FDA doivent renouveler leurs enregistrements avant le 31 décembre  

                            Renouveler Maintenant

                            Rappel

                            L’U.S. Food and Drug Administration (FDA) exige que tous les établissements agro-alimentaires, pharmaceutiques, et de dispositifs médicaux leurs enregistrements FDA entre le 1er octobre et le 31 décembre

                            Renouveler Maintenant

                            Attention

                            La période de renouvellement de l’U.S. FDA est TERMINEE depuis le 31 décembre

                            Si vous n’avez pas renouvelé avant la date limite, vous devez vous réenregistrer auprès de la FDA.

                            Réenregistrez-vous ou vérifiez que votre enregistrement a été renouvelé pour :

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                            Obtenez 18 mois de service d’enregistrement et d’agent U.S. au tarif de 12 si vous vous enregistrez aujourd’hui.

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