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Registrar

Assistance with U.S. FDA Regulations

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MyFDA Monitor

FSMA Made Easy

Simplify FSVP compliance using the FDA Compliance Monitor

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

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

Get a Quote

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.

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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.

                            Topnotch 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.

                            Learn More

                            Transform Your Supplier Discovery with Marketplace

                            • Source global suppliers 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

                            See how much you can save
                            • Monitor + DMS

                            5 Facilities

                            $133/month

                            • $27.00/month per facility

                            10 Facilities

                            $200/month

                            • $20.00/month per facility

                            25 Facilities

                            $400/month

                            • $16.00/month per facility

                            25+ Facilities

                            Custom Pricing

                            • Reach out for a custom plan

                            Not seeing the right plan for your business?

                            Supplier Monitoring Is Required Under FSMA

                            FDA FSVP Rule

                            Deadlines Passed March 19, 2018

                            FDA’s Foreign Supplier Verification Program (FSVP) rule requires food importers to conduct and document an evaluation of their foreign suppliers’ FDA compliance status, “including whether the foreign supplier is the subject of an FDA warning letter, import alert, or other FDA compliance action related to food safety.” This requirement cannot be fulfilled by your customs broker.

                            VIEW FDA’s FSVP RULE

                            FDA Preventive Controls Rule

                            Deadlines Passed September 18, 2017

                            FDA’s Preventive Controls Rules require registered food facilities to establish, implement and document a supply-chain program monitoring their suppliers’ FDA compliance status, “including an FDA warning letter or import alert relating to the safety of food and other FDA compliance actions…”

                            VIEW FDA’s PREVENTIVE CONTROLS RULE

                            Streamline compliance using the FDA Compliance Monitor.

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

                            Soluzioni

                            Registrazione FDA

                            FDA Compliance Monitor

                            Etichettatura secondo la normativa FDA

                            Visualizzate tutto

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                            144 Research Drive Hampton, Virginia 23666 USA
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                            Avviso: Le aziende che non hanno rinnovato la registrazione FDA nel   devono ri-registrarsi.

                            Avviso: Le aziende farmaceutiche e di dispositivi medici che non hanno rinnovato la registrazione FDA nel   devono ri-registrarsi.

                            Ri-registratevi ora

                            Le aziende registrate alla FDA devono rinnovare le proprie registrazioni entro il 31 dicembre  

                            Le aziende farmaceutiche e di dispositivi medici devono rinnovare le proprie registrazioni entro il 31 dicembre  

                            Rinnovate ora

                            Promemoria

                            La U.S. Food and Drug Administration (FDA) richiede che tutte le aziende alimentari, farmaceutiche e di dispostivi medici rinnovino le proprie registrazioni FDA tra il 1° ottobre e il 31 dicembre

                            Rinnovate ora

                            Avviso

                            Il periodo di rinnovo per la registrazione alla U.S. FDA è TERMINATO il 31 dicembre

                            Se non avete rinnovato entro la scadenza, dovete ri-registrarvi presso la FDA.

                            Ri-registratevi o verificate se la vostra registrazione è stata rinnovata per il :

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                            Se vi registrate oggi, otterrete 18 mesi di registrazione e servizio Agente U.S. al prezzo di 12

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