U.S. Agent Services for Drugs & Pharma

U.S. Agent Services Drugs & Pharma

Official Communication Hub

As your designated U.S. Agent, we act as the mandatory, primary FDA contact. All official correspondence, regulatory notices, and inquiries are received and forwarded to your team.

  • Primary FDA point of contact
  • DRLS system communications managed
  • No missed notices due to time zones or language
  • Regulatory inquiry handling

Inspection Coordination

We facilitate and coordinate FDA facility inspections for your drug establishment managing logistics and ensuring you are fully prepared for every visit.

  • FDA inspection scheduling support
  • Logistics coordination with your team
  • Pre-inspection readiness guidance
  • Post-inspection follow-up

Emergency Contact

For drug recalls, safety alerts, or public health emergencies, the FDA contacts us immediately ensuring your team is notified and can respond without delay.

  • Recall & public health alert response
  • Rapid notification to your team
  • Protects company & public safety

Registration & Annual Support

We assist with drug establishment registration, DUNS number maintenance, drug product listing, and all annual renewal requirements.

  • Drug establishment registration
  • Annual renewal coordination
  • DUNS number maintenance
  • Drug product listing (NDC) support

Your Dedicated FDA Partner for Pharmaceuticals

From OTC drugs to prescription pharmaceuticals, our team understands the complexity of FDA drug regulations. Choosing the right U.S. Agent means partnering with experts who provide the personal attention your compliance demands.


Drugs & Pharma Services At a Glance

ServiceWho Needs ItFrequencyTimeframePricing
Starting at
U.S. Agent ServicesForeign facilities onlyAnnualBefore FDA registration; renew each year$295/yr
Drug Establishment RegistrationDomestic & foreignAnnualOctober-December of each year$449/yr
Drug Product Listing (NDC)All drug manufacturersAnnual + per changeAt registration; updated when products change$299/product
Structured Product Labeling (SPL)All drug manufacturersPer submissionAt listing submission & with each label update$249/submission
Drug Label ReviewAll manufacturersPer product/changeBefore market entry or label revision$449/product
Animal & Veterinary DrugsVet drug manufacturersAnnualOctober-December of each year$449/yr

US Agent Drugs & Pharma FAQs

What does a U.S. Agent do for a foreign drug establishment?

A U.S. Agent is the FDA’s official point of contact for a foreign drug or pharmaceutical establishment. That means receiving and routing all FDA communications, helping coordinate facility inspections, and being reachable during U.S. business hours, year-round.

Is a U.S. Agent required for foreign drug manufacturers?

Yes. Under 21 CFR Part 207, a foreign drug establishment must designate a U.S. Agent before it can register with the FDA. The agent must have a physical U.S. address and be available during normal business hours; a P.O. box doesn’t qualify.

How does the U.S. Agent handle FDA inspections?

We help schedule inspections, coordinate logistics with your team, and provide pre-inspection readiness guidance so your facility isn’t caught off guard, plus manage post-inspection follow-up communications with the FDA.

What happens during a drug recall or safety alert?

The FDA contacts the U.S. Agent first. We’re available to receive that notification and relay it to your team immediately, so there’s no delay in responding to a recall or public health alert.