Regulatory Compliance

EOF Notification for Dietary Supplements: Complete Guide

What it takes to legally place a dietary supplement on the Greek market — procedure, documents, timeline, and how responsibilities are divided.

Swiss Formula is a European private label dietary supplement manufacturing company providing formulation development, manufacturing, packaging and regulatory support through a network of GMP-certified manufacturing facilities across Europe and Switzerland.

Last updated: June 2026  ·  Content curated by Giannis Moutafidis, Founder & CEO, Swiss Formula

What Is the EOF Notification

To place a dietary supplement on the Greek market, legalization for market placement is required from the National Organization for Medicines (EOF), in accordance with Directive 2002/46/EC. The procedure ensures that the product is legal, safe, and compliant with Greek and European legislation.

Without an EOF notification number, a dietary supplement cannot be legally sold in Greece — not in pharmacies, not online, and not through healthcare professionals.

What the Notification Dossier Includes

The dossier submitted to EOF must include the following:

Product detailsBrand name, format, ingredients, dosage
Composition and formula descriptionFull breakdown of raw materials and quantities
Raw material certificationsQuality and origin documentation for ingredients
Label and packaging informationIncluding health claims in accordance with EC Regulation 1924/2006
Stability & quality control reportsDocumentation of product shelf life and safety

Indicative Timeline

The overall process — from formula approval to delivery of the finished product — follows roughly this timeline:

Wk 0-1

Formula selection & label design

Client approval of design mockups

Wk 2-3

Production scheduling

Formula materials sent to the factory

Wk 4-5

Final approval & dossier submission

Fee payment and notification submission to EOF

Wk 6-7

Notification received

EOF notification number issued

Wk 8-12

Manufacturing, packaging & delivery

Finished product ready, with the notification number printed on the label

How Responsibilities Are Divided

In a private label or white label partnership, roles are clear from the start:

The Client (Brand Owner)

Approves the final label and the content of health claims in writing, as well as any form of promotion for their product.

We (Brand Developer)

Ensure that manufacturing complies with GMP, and handle the preparation and submission of the notification dossier to EOF.

This division of responsibilities is clearly defined in a written partnership agreement before production begins — so you know from the outset who does what.

We deliver your product ready to sell, with EOF notification complete

We cover the entire process — from formula to EOF notification number.

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