• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • +1-757-224-0177
  • Contact Us
  • MyFDA Login
  • COVID-19 PPE
  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
Registrar

Registrar

Assistance with U.S. FDA Regulations

  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
  • FDA Registration
  • Services
    • FDA Registration
    • Cosmetics FDA Registration
    • U.S. FDA Detention Assistance
    • Food Safety and FSMA
    • FDA Labeling
    • UDI and GUDID
    • Master Files
    • GACC Registration
    • Unique Facility Identifier (UFI)
    • U.S. FDA Export Certificate Requirements
    • TTB Registration
  • Products
    • FDA Compliance Monitor
      • Buyer Insights
      • Marketplace
      • Exporter Marketplace
    • Cosmetri
    • A la Calc
    • Online Training
  • Our Brands
    • Cosmetri
    • A la Calc
  • Industries
    • Food and Beverages
    • Dietary Supplements
    • Medical Devices
    • Drugs
    • Cosmetics
    • Other
  • Resources
    • Resources
    • Regulatory News
    • Events / Webinars
    • Partners
    • Free Tools
  • About Us
    • About
    • Contact Us
    • Careers

U.S. FDA 3PL/WDD Reporting

U.S. FDA 3PL/WDD Reporting

U.S. FDA requires Third-Party Logistics (3PL) providers and Wholesale Drug Distributors (WDD) to report state licensure and other information for all of their facilities between January 1 and March 31 of each year.  Among other things, reports must include any significant disciplinary actions taken against the facilities by a state or federal agency.

For assistance with 3PL/WDD reporting requirements, simply complete the form below:

  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • Provide your company information

  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • 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.

  • Drop files here or
    Max. file size: 50 MB.
    • Drop files here or
      Max. file size: 50 MB.
      • 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
      • This field is hidden when viewing the form
      • (11 Digit Number)
      • (Please indicate capital letters)
      • Compliance Information

      •  
      • Drop files here or
        Max. file size: 50 MB.
        • Drop files here or
          Max. file size: 50 MB.
          • Max. file size: 15 MB.
          • Max. file size: 15 MB.
          • Drop files here or
            Max. file size: 15 MB, Max. files: 10.
            • Drop files here or
              Max. file size: 15 MB.
              • Drop files here or
                Max. file size: 15 MB.
                • Drop files here or
                  Max. file size: 15 MB.
                  • Drop files here or
                    Max. file size: 15 MB.

                    • Provide the following information for each of your NIOSH approved respirators
                      Manufacturer NameModel NumberNIOSH Approval Number 
                    • Drop files here or
                      Max. file size: 50 MB.
                      • Issued by another regulatory authority or conformity assessment body. Include the authorization number and name of the assessment body (if applicable)
                        Drop files here or
                        Max. file size: 50 MB.
                        •  
                          Drop files here or
                          Max. file size: 50 MB.
                          • Report should demonstrate applicable performance standards have been met
                            Drop files here or
                            Max. file size: 50 MB.

                            Primary Sidebar

                            Connect With Us

                             

                            144 Research Drive

                            Hampton, Virginia 23666 USA

                             

                            +1-757-224-0177 

                             

                            +1-757-224-0179

                             

                            [email protected]

                             
                             
                             
                             

                            OUR LOCATIONS

                            24/7 LIVE CHAT

                            Solutions

                            FDA Registration

                            FDA Compliance Monitor

                            FDA Labeling

                            View All

                            About

                            About Us

                            Resources

                            Free Tools

                            Fees

                            Contact Us

                             

                            Reviews

                            Locations

                            Events

                            Associations

                            Careers

                            Phone: +1-757-224-0177

                            Fax: +1-757-224-0179

                            [email protected]

                            © 2025 Registrar Corp

                            144 Research Drive Hampton, Virginia 23666 USA
                            Terms of Use | Privacy Policy

                            • English
                              • Español
                              • Italiano
                              • Deutsch
                              • Français
                              • 中文
                              • Portuguese
                              • 日本語
                              • Back
                            • FDA Registration
                            • Services
                              • FDA Registration
                              • Cosmetics FDA Registration
                              • U.S. FDA Detention Assistance
                              • Food Safety and FSMA
                              • FDA Labeling
                              • UDI and GUDID
                              • Master Files
                              • GACC Registration
                              • Unique Facility Identifier (UFI)
                              • U.S. FDA Export Certificate Requirements
                              • TTB Registration
                              • Back
                            • Products
                              • FDA Compliance Monitor
                                • Buyer Insights
                                • Marketplace
                                • Exporter Marketplace
                                • Back
                              • Cosmetri
                              • A la Calc
                              • Online Training
                              • Back
                            • Our Brands
                              • Cosmetri
                              • A la Calc
                              • Back
                            • Industries
                              • Food and Beverages
                              • Dietary Supplements
                              • Medical Devices
                              • Drugs
                              • Cosmetics
                              • Other
                              • Back
                            • Resources
                              • Resources
                              • Regulatory News
                              • Events / Webinars
                              • Partners
                              • Free Tools
                              • Back
                            • About Us
                              • About
                              • Contact Us
                              • Careers
                              • Back

                            FDA has cancelled thousands of registrations that were not properly renewed or did not include
                            an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

                            Notice: Medical Device and Drug establishments that did not renew their FDA registrations in   must re-register.


                            Get Help Now

                            FDA-registered facilities must renew their registrations by December 31,  

                            Medical Device and Drug establishments must renew their registrations by December 31,  

                            Renew Now

                            Reminder

                            The U.S. Food and Drug Administration (FDA) requires that all registered food, medical device, and drug facilities renew their FDA registration between October 1 and December 31,

                            Renew Now

                            Notice

                            The U.S. FDA Registration Renewal period CLOSED on December 31,

                            If you did not renew by the deadline, you must re-register with FDA.

                            Re-register or verify that your registration was renewed for :

                            Re-Register
                            Verify

                            Limited Time Offer

                            Get 18 Months of Registration and U.S. Agent service for the price of 12 when you sign up today.

                            Get Started
                            Open Modal