Consumer Protection Law and Regulations

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Consumer protection law thought leadership, articles, podcasts, videos and webinars from expert sources across the legal world. Explore insights covering topics that involve consumer protection regulations and the developing law surrounding them from specialists working in this area.
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.
Worldwide Consumer
AP
Arnold & Porter
Article
Updates On The Federal Competition And Consumer Protection Commission’s (FCCPC) Recent Activities And Other Developments In The Consumer Protection Sector
The Federal Competition and Consumer Protection Commission (FCCPC) has announced that all payments for services provided by the Commission must now be made through the RevOp platform, a new revenue collection platform introduced by the Federal Government. The Commission outlined a step-by-step process for generating a bill and completing payment through the new platform, including payment by bank transfer, card, or at a bank branch.
Nigeria Consumer
SA
S.P.A. Ajibade & Co.
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.
Afghanistan Consumer
AP
Arnold & Porter
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Article
South Africa’s Opt-Out Registry: This Is An IT Project, Not Just A Legal One
South Africa's National Consumer Commission Opt-Out Registry introduces a dual compliance framework that requires organisations to satisfy both POPIA's personal information processing requirements and the CPA's pre-emptive marketing blocks. Businesses must fundamentally restructure their technology, data management, and operational processes to prevent prohibited marketing communications from reaching consumers who have exercised their right to opt out.
South Africa Media & IT
E
ENS
Article
AI Regulation In The EU And Nigeria: AI Watermarking
The European Union's AI Act introduces mandatory watermarking requirements for AI-generated content, creating compliance obligations that extend beyond EU borders to affect Nigerian businesses using global AI services. This analysis examines how these transparency requirements intersect with Nigeria's existing regulatory framework and highlights the need for comprehensive AI governance legislation.
Worldwide Technology
PL
Pavestones Legal
Article
DSA Risk Assessment Failures: Lessons From The €550M AliExpress Decision
The European Commission has imposed a €550 million fine on AliExpress for Digital Services Act violations, marking the largest penalty under the DSA to date. The decision reveals critical failures in risk assessment methodology, moderation resourcing, and enforcement of seller penalties that allowed illegal products to proliferate on the platform. This landmark case establishes new compliance expectations for marketplaces regarding systemic risk management and operational controls.
Afghanistan Media & IT
LP
Logan & Partners
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Article
Côte D’Ivoire Hosts Fourth Africa GI Training Programme
The African Organisation of Intellectual Property (OAPI) has initiated its fourth Africa GI Training programme in Abidjan, bringing together participants from 13 member states to develop expertise in geographical indications. This capacity-building initiative combines theoretical learning with practical application to strengthen the protection and promotion of local products across the continent. The programme represents a strategic effort to leverage geographical indications as instruments for economic dev
Cote D'ivoire IP
AA
Adams & Adams
Article
Law And Development: Building The Legal Architecture For Nigeria’s Industrialisation
Nigeria's development trajectory depends critically on modern legal frameworks that can attract investment, reduce risk, and create the institutional certainty necessary for economic transformation. This analysis examines how deliberate legal reform in sectors like electricity, education, healthcare, and infrastructure can serve as strategic tools for industrialization, drawing lessons from China's reform architecture and Rwanda's regulatory overhaul.
Worldwide Government
OA
Olisa Agbakoba Legal (OAL)
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Article
Cleanse Or Consent? The ZAR0.12 Question Every South African Direct Marketer Must Answer
ENSafrica's latest legal bulletin examines critical regulatory shifts across Africa, from South Africa's mandatory monthly opt-out cleansing under amended CPA rules to Rwanda's new VAT framework for cross-border digital services. The collection addresses constitutional interpretation in Ghana, AI policy governance failures, merger threshold updates, and emerging challenges in crypto regulation and prediction markets.
South Africa Consumer
E
ENS
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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.
Worldwide Consumer
AP
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.
Afghanistan Consumer
AP
Arnold & Porter
See more