Your fastest, safest path into the Saudi market.

SFDA registration and GSO standards compliance are not formalities — they are the gate to one of the region's fastest-growing nutrition and medical markets. We guide manufacturers through registration, classification, and approval, so you don't learn the system the hard way.

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Backed by hands-on submission experience across infant nutrition, supplements, and medical nutrition categories — not theoretical knowledge of the regulations, but a track record of approvals.

What We Register

Four regulated categories, one disciplined process.

Infant Formula

Infant formula carries the strictest scrutiny of any regulated nutrition category — and the least room for error. Get your infant formula registration right from the start.

Technical Documentation — complete dossiers to SFDA & GSO 2106 standards
Age-Classification Strategy — precise categorization to avoid rejection
Label Compliance — bilingual, SFDA-compliant labeling review
Government Communication — end-to-end SFDA liaison

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Infant Nutrition

From follow-on formula to complementary infant foods, each category carries its own classification rules and claim restrictions.

Product Classification — follow-on formula & complementary foods
Technical Documentation — submission-ready dossiers
Claim Restriction Guidance — what can and cannot be claimed
Approval Support — end-to-end guidance to approval

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Food Supplements

Supplement approval hinges on correct classification, substantiated claims, and precise labeling. Registration without the guesswork.

Product Classification — right regulatory pathway from the start
Substantiated Claims Review — defensible, compliant claims
Label Compliance — bilingual labeling in line with formulation
Post-Registration Support — product changes, label updates and compliance questions as agreed

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Medical Nutrition

Products at the intersection of food regulation and clinical use, requiring clear classification, evidence and compliant claims.

Product Classification — pathway based on formulation, intended use and claims
Technical Documentation — evidence prepared for the applicable pathway
Claims Compliance — claims managed within the agreed scope
SFDA Submission Management — registration review and next steps

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HOW REGISTRATION WORKS

A clear, five-step path from product to approval.

Initial Assessment
We review your product, formulation, and target category to confirm the correct regulatory pathway before any paperwork begins.
Classification & Documentation
We determine the appropriate regulatory pathway and manage the classification and documentation work required for the submission.
Label & Claims Review
Every claim and label element is checked against current regulations before submission — this is where most rejections are prevented.
Submission & Government Liaison
We submit on your behalf and manage all communication with the SFDA throughout the review period.
Registration Outcome & Market-Entry Next Steps
After the registration outcome, we manage the next steps within the agreed scope, including any remaining product, labelling and shipment-clearance requirements relevant to your case.

Ready to start the process?

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FREQUENTLY ASKED QUESTIONS

Questions we hear most from manufacturers.

How long does SFDA registration typically take?

Timelines vary by product category and completeness of documentation. We'll give you a specific estimate for your product during the initial assessment, rather than a generic industry-wide number.

Which product categories do you register?

Infant Formula, Infant Nutrition, Food Supplements, and Medical Nutrition. If your product falls outside these categories, let us know and we'll advise honestly on whether we're the right fit.

Do you handle both new registrations and renewals?

Yes — we manage initial registrations, renewals and variation submissions where they apply, helping you maintain compliance over time.

FAQs

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