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  • Article

    Poison Centre Notification Compliance: Distributor Obligations And Clarification Of UFI Requirements For Imported Mixtures

    Starting January 2027, the Classification, Labelling and Packaging Regulation will explicitly designate distributors as duty holders, fundamentally changing how companies manage Poison Centre Notification requirements across the European Union supply chain. This regulatory clarification particularly impacts businesses that sell mixtures not covered by existing notifications or rebrand products under their own labels. Companies must now assess whether their current compliance framework adequately addresses t
    AfghanistanConsumer Protection
    Bergeson & Campbell
    Bergeson & Campbell
  • Article

    European Commission Fines AliExpress €550million, Emphasising E-commerce Platforms' Responsibilities To Consumers

    In particular, the Commission held that the platform failed to assess staffing requirements for the review of potentially illegal products, how its advertising systems were contributing to the proliferation of illegal products, and how well its systems prevented the risk of illegal products appearing or being re-listed.
AfghanistanConsumer Protection
Marks & Clerk
Marks & Clerk
  • Article

    European Commission Fines Temu €200 Million For Breaching The Digital Services Act

    The European Commission has imposed a €200 million fine on Temu for failing to properly assess the risk of illegal products on its platform, marking a major enforcement action under the Digital Services Act.
    European UnionConsumer Protection
    Lewis Silkin
    Lewis Silkin
  • Article

    CJEU Ruling Clarifies Scope Of Medical Device Definition

    The Court of Justice of the European Union has issued a preliminary ruling in Case C-427/24 Diagramm Halbach, establishing critical principles for determining whether products qualify as medical devices under the EU Medical Device Regulation. The judgment clarifies that manufacturer advertising alone does not determine medical device status, and that products must objectively perform medical purposes to fall within the regulatory definition.
    GlobalConsumer Protection
    Arnold & Porter
    Arnold & Porter
  • Article

    The EU Packaging And Packaging Waste Regulation: Why Life Sciences Companies Should Act Now

    The EU Packaging and Packaging Waste Regulation becomes applicable on 12 August 2026, replacing existing directives with a directly applicable regime governing packaging design, documentation, labelling and end-of-life management across the EU market. Life sciences companies manufacturing medical devices, IVDs and pharmaceuticals face significant compliance obligations, with narrow sector-specific exemptions that do not eliminate core requirements for conformity documentation, substance restrictions...
    AfghanistanConsumer Protection
    Arnold & Porter
    Arnold & Porter
  • Article

    How Will The EU Parliament Shape The MDR/IVDR Revision? Draft Report Indicates How Parliament May Seek To Amend Commission’s Proposals

    The European Parliament's draft report proposes over 130 amendments to the Commission's plan for overhauling medical device regulations, introducing new categories like "niche" devices while expanding coordination mechanisms between EU authorities. These changes aim to balance regulatory simplification with patient safety, potentially reshaping how medical devices and in vitro diagnostics are classified, assessed, and brought to market across the European Union.
    AfghanistanConsumer Protection
    Arnold & Porter
    Arnold & Porter
  • Article

    Who’s Liable Now? How The EU’s New Product Liability Directive Expands The Net

    The EU's Product Liability Directive has been modernised to reflect today's complex supply chains, expanding liability beyond manufacturers to include online platforms, fulfilment providers, and other economic operators.
    AfghanistanConsumer Protection
    Logan & Partners
    Logan & Partners
  • Showing 1–7 of 7 results

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