Trade compliance consulting, since 2018.
KGP FDA
Registration, representation and labeling in the US, Canada, the EU and the UK for food, dietary supplement, cosmetic, drug and medical device manufacturers.
Tell us your product and target market; we send a preliminary assessment within 24 hours.
Free Preliminary AssessmentChoose Your Market
60
services across five market pages
- Food and beverages
- Dietary supplements
- Cosmetics
- Drugs
- Medical devices
- Animal-origin products
Fees are listed in each market page’s fee table; government agency fees are shown separately.
Four Steps, One Point of Contact
Whatever the market or product group, you know what will be done, what you will receive and what it costs before work begins.
Needs assessment
We learn about your product, your target market and your importer’s role, then identify which registration, representation and labeling obligations fall to you.
Proposal
We send the scope and fee within 24 hours. Where government agencies charge their own fees, the proposal shows them separately.
Filing and preparation
We file registrations on your behalf, prepare label and product files, and act as your appointed representative where the market requires one.
Follow-up and updates
We track renewal dates for you. For registration services, information updates and corrections within the calendar year are included.
On the Exporter’s Side Since 2018
KGP FDA helps food, dietary supplement, cosmetic, drug and medical device manufacturers enter four markets in compliance. Since 2018 we have worked with more than 500 companies from many countries.
On the registration and representation side we handle facility registrations, US Agent service, product listings and the EU and UK Responsible Person role. On the product side we prepare labels, nutrition facts, allergen assessments and cosmetic files.
US · Canada · EU · UK
- Founded
- 2018
- Markets
- US, Canada, EU, UK
- Response
- Within 24 hours
- Support line
- 24/7
Frequently Asked Questions
Which markets do you cover?
The United States, Canada, the European Union and the United Kingdom. Technical services such as label preparation, nutrition facts calculation and regulatory dossiers apply to all four markets. Each market’s service list is on its own page: United States, Canada, European Union, United Kingdom.
How quickly do you respond?
We respond to every request within 24 hours and can be reached 24/7. How long an application takes at the government agency depends on the agency and the service; we state that time separately in the proposal.
Are information changes or corrections after registration charged?
For registration services, information updates and corrections within the calendar year are included. We also track renewal periods and let you know before they come due.
Where can I see the fees?
In the “Services and fees” table at the end of each market page. For services without a listed fee we prepare a proposal. Government agencies’ own fees (for example, FDA’s annual fee for medical device establishment registration) are not included in our consulting fee and are shown separately in the proposal.
Tell Us About Your Product and Market
We assess, free of charge, which registration, representation and labeling work you need, and reply within 24 hours.
Phone and WhatsApp +1 917 960 9666 · info@kgpfda.com