Selling food supplements online in the EU follows the same food law as in-store sales. This guide covers notification, labelling, mandatory product page information, permitted ingredients and claims in 2026.
Other Industries
AliExpress Fined €550 Million Under the DSA: What Marketplace Enforcement Means for Manufacturers
The European Commission’s €550 million fine against AliExpress under the Digital Services Act marks a major shift in marketplace enforcement. While the decision targets the platform, manufacturers and sellers should expect stricter compliance checks, stronger product verification requirements, and greater scrutiny when selling products in the EU.
PPWR: The New EU Packaging Regulation Taking Effect in August 2026
Starting 12 August 2026, the EU’s new Packaging and Packaging Waste Regulation (PPWR) replaces Directive 94/62/EC with a single, harmonized law across all 27 Member States. Applying to all economic operators—including manufacturers, importers, and online marketplaces—the PPWR introduces immediate requirements from day one with no grace period, including PFAS restrictions on food-contact packaging, technical documentation, tracking information, and EU Declarations of Conformity for all packaging formats.
Key Differences Between FBO Registration and Cosmetic Responsible Persons in 2026
Food and cosmetics fall under two distinct legal frameworks, each with its regulatory requirements and obligations.
This article outlines the key differences between the Food Business Operator (FBO) and the Cosmetic Responsible Person (RP), and explains how these roles apply differently to products entering the European market in 2026.
The EU’s first major DSA enforcement action is a warning sign that compliance can no longer be an afterthought
With the first landmark penalty officially issued under the Digital Services Act, Very Large Online Platforms selling in Europe must immediately audit their compliance strategies to mitigate massive financial and reputational risks.
Obelis Group Partners with IBA to Keep Beauty Brands Ahead of U.S. Cosmetic Regulations
Through our partnership with the Independent Beauty Association and our sponsorship of the Fiscal Note U.S. Policy Map, we equip beauty brands with real-time regulatory insights and expert support, helping them stay compliant with MoCRA and confidently navigate the U.S. market.
Leading Through Complexity: Doram Elkayam, on Multi-Market Compliance and the Road to 2026
Obelis COO Doram Elkayam shares how he navigates complex EU, UK, US, Swiss and Canadian regulations to streamline multi-market access for medical devices, IVDs, cosmetics and more. In this interview, he reflects on 2025, key trends for 2026, and why smart regulatory strategy is now a business essential.
New Restriction on Homosalate in Cosmetics Comes into Effect on 1 July 2025
From 1 July 2025, the EU will enforce new limits on Homosalate in cosmetics, allowing a max of 7.34% in face products. Reformulation may be required to ensure compliance.
Canadian In-Country Representative Requirement for Cosmetics
Discover Health Canada’s update requiring a Canadian-based representative for foreign cosmetic brands and how Obelis can help with compliance.
EU PMS requirements for medical devices under scrutiny of Dutch authority
Dutch audits reveal non-compliance with EU post-market surveillance (PMS) requirements for medical devices. Learn how to strengthen PMS systems for compliance and safety.