• Skip to primary navigation
  • Skip to main content
  • +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

FDA Compliance Monitor: Calculate Your Savings

How much will you save with the FDA Compliance Monitor?

Automate supply chain risk management with the FDA Compliance Monitor, a modern, flexible solution for addressing your supplier verification and approval requirements under FSMA.

Get a Quote
Schedule a Demo

Enter your supplier count below to see how much it can help you save annually.

Estimated Savings:  

Include Document Management

Read below to learn how

Supplier Monitoring

Under FSMA, U.S. importers are required to monitor their foreign suppliers’ FDA compliance history.  This work may involve:

  hours per supplier per year

Estimated effort to research, document, and approve suppliers in compliance with FSVP requirements

$  / hour

Estimated full-time rate for work, based on Food Safety supervisor average annual salary of $57,773

The FDA Compliance monitor can save you   in labor costs associated with fulfilling FSMA monitoring requirements for   suppliers.

Document Management

Under FSMA, U.S. Importers are required to verify and approve their suppliers FDA compliance.  This work may involve:

  hours per supplier per month

Estimated effort to manage document collection, tracking, review, and approval

$  / hour

Based on Food Safety supervisor average annual salary of $57,773

The FDA Compliance Monitor’s Document Management System can save you   in annual labor costs for managing and approving documentation for   suppliers.

Cost Avoidance

Manual supplier monitoring processes leave room for human error that can cause unanticipated turbulence and costs.  These may include:

$  per detention

Estimated based on freight transfers, delay and storage fees, re-export and disposal costs over the span of weeks.

$  / hour for   hours per week across   weeks

Additional labor to address routine compliance responsibilities in a non-automated system.

The FDA Compliance monitor can save you   in unanticipated costs associated with addressing compliance issues and maintaining routine compliance work.

Risk Mitigation

Regular changes in your supply-chain produce a need to research supplier risk before purchase.  This work may involve:

$  labor costs

Estimated based on a   annual change in supplier sources with   hours of labor spent on approval processes per new supplier at $  per hour

$  labor cost

One week of regular work to maintain compliance done by key personnel at $  per hour.

The FDA Compliance monitor can save you   in annual labor costs associated with sourcing new suppliers.

 

Hidden annual costs without the FDA Compliance Monitor

–

 

Cost of the FDA Compliance Monitor and Document Management for   suppliers

=

 

Estimated annual savings

Save   in annual costs with the FDA Compliance Monitor

Start Monitoring Schedule a Demo

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