L. de Brouwer "Le droit des jeux plublicitaires", Larcier, 2016.

Parmi les méthodes de promotion des ventes, les jeux publicitaires occupent une place singulière : les loteries, tombolas, jeux et concours publicitaires n’offrent en effet au consommateur que l’espoir d’un gain, mais chargé, il est vrai, d’un pouvoir attractif souvent convaincant.

Les nombreuses règles légales qui les gouvernent se situent à la croisée de deux secteurs d’activités réglementés de manière presque antinomique : d’un côté, les loteries et les jeux de hasard sur lesquels l’État exerce un monopole et un contrôle souverain ; de l’autre, le commerce où règnent les principes de liberté et de libre concurrence, mais encadrés par les dispositions protectrices des consommateurs.

La mise en œuvre d’un jeu publicitaire oblige son organisateur à se poser des questions essentielles avant de porter son choix sur l’une ou l’autre formule : concours ou loterie ? jeu ou jeu de hasard ? opération à lancer sur des supports classiques, on air ou on line, via un site internet ou des réseaux sociaux ? lots en espèces ou en nature ? intervention d’un huissier de justice ? risque de disqualification ? Quant à la rédaction du règlement,
il soulève d’autres questions : les clauses sont-elles toujours licites, pertinentes et opposables à chacun des participants ?

Le lecteur trouvera dans le présent ouvrage des réponses aux multiples questions que posent le choix, la mise en œuvre et la gestion des jeux publicitaires. L’ensemble des règles qui leur sont applicables sont exposées d’une manière ordonnée et synthétique, ce qui n’exclut ni l’approfondissement ni la critique. Les nombreux exemples pratiques, tous tirés de la jurisprudence, illustrent le commentaire. À dessein, l’auteur utilise un langage clair et accessible à tous ceux auxquels l’ouvrage s’adresse : les professionnels de la communication et du marketing, les juristes et les joueurs.

http://editionslarcier.larciergroup.com/titres/133385_2_0/le-droit-des-jeux-publicitaires.html

 

Within the European Union, the rules on processing personal data are still governed by the Directive 1995/46/EC. These rules were conceived before the era of social networks, big data and the Internet of things, and were often misunderstood and misapplied by companies and organizations. Its revision has been at the agenda since 2012. After several years of intensive discussions, a final text was finally adopted in December 2015. It should be voted by the European Union legislator and published in the Official Journal in the following weeks.
The modernization of the system of protection of personal data should have important practical consequences for most companies and organizations. In particular, those who, within these organizations, are responsible for ensuring the respect of the rules, will be faced with new multiple challenges. It is not only about applying new legal requirements, carrying out new administrative procedures or adapting the  phrasing  of some clauses of general conditions or privacy policies. The requirements of the regulation, mainly through the concept called "accountability", go well beyond that.
In this document we give a complete overview of these new obligations, but also of new powers which will be allocated to the regulator, at a national and at the European level. These powers can result in investigations and investigative measures, positive injunctions and even administrative fines.

pdfGDPR_Note_Generale_SimontBraun_Janv_2016.pdf

 

Publication of the book “Actualités en droits intellectuels” under the coordination of Benjamin Docquir

This book includes two studies authored by lawyers of Simont Braun : Philippe Campolini discusses the recent developments on the creation of a European patent with unitary effect and the future Unified Patent Court, and Benjamin Docquir (in collaboration with Edouard Cruysmans) examines the limits of copyright in the digital environment, in particular the exceptions for research and e-learning, the private copying levies, etc

The book also reports on several other topics of great relevance in the field of intellectual property rights: the proposal for a Directive on business secrets, the recent case law of the European Court of justice on registered designs, customs measures, injunctions under the new Code of economic law, etc.

For more information: http://fr.bruylant.larciergroup.com/titres/132250_2/actualites-en-droits-intellectuels.html

 

Pursuant to article 1, §1 and article 3 §3 of the Law of 30 June 1994 concerning copyrights and neighbouring rights (hereafter: Author Rights):

  • the author of a literary or artistic work has the exclusive right to reproduce the work or to authorize reproduction by any means andin any form (whether directly or indirectly, temporarily or permanently, or in whole or in part) ; and
  • the author may assign the Author Rights with respect to the works created by an author in the execution of an employment contract or a statutory function to the employer, provided (i) that the transfer of Author Rights is expressly agreed and (ii) that the creation of the work is within the scope of the employment contract or statutory function.

The transfer of these Author Rights is sometimes remunerated. Until recently, the tax and social security treatment of this income was unclear.

The Belgian rules on invention patents underwent certain changes in 2011, one of which was the introduction of a restoration procedure (1).  This restoration procedure, which came into effect on 13 March 2014, allows applicants for or holders of patents that missed a deadline in procedures before the Belgian Office for Intellectual Property (OPRI), to commence proceedings before it aimed at restoring the rights lost owing to the failure. The main cases in contemplation are failure to meet the deadline for paying the annual taxes or that for filing a translation of a European patent (which, for some time now, has only concerned European patents issued in English).

THE SUPREME COURT ORDERS A COMPLETE, DETAILED EXAMINATION OF THE  PRIMA FACIE VALIDITY OF THE PATENT INVOKED IN SUPPORT OF A REQUEST FOR A COUNTERFEIT SEIZURE

Supreme Court, 12 September 2014, Syral Belgium v. Roquette Frères, C.13.0232.N, available here.

TEXT AND CONTEXT

Section 1369bis/1 of the Belgian Judicial Code provides that the court ruling on a petition for a counterfeit seizure must examine the prima facie validity of the intellectual property right invoked.

In order to challenge this prima facie validity, defendants frequently cite cases in which the patent relied on has already been ruled to be void. These may be either first instance decisions that are not yet final (otherwise, were the patent to be finally set aside, it could not be founded on for a counterfeit seizure petition) or foreign decisions whose grounds the defendant argues must apply by analogy to the patent relied on in Belgium.

However, challenging the prima facie validity of a patent based on a decision from foreign court or that is not res iudicata is often no easy task. Based on the rule that issued patents are in principle to be considered valid, the Belgian courts often reject such arguments on the ground that a patent is to be considered valid until revoked by a final decision or, at least, one that is provisionally enforceable. Foreign decisions are often rejected outright by the court on the ground – correct in and of itself, though questionable as to its relevance – that they relate to foreign rights that are of no effect in Belgium.

EUROPEAN COURT OF JUSTICE AFFIRMS STRONG PROTECTION FOR COMMUNITY DESIGN
 
Court of Justice 19 June 2014, Karen Millen Fashions Ltd. vs Dunnes Stores & Dunnes Stores (Limerick) Ltd.,C/345-13, click here


TEXT & CONTEXT :
 
Karen Millen Fashion (in short “KMF”),  is an English brand that produces and sells women’s clothing. In 2005 KMF designed and sold in Ireland a striped shirt and a black knit top. Dunnes, a retailing group in Ireland that also sells women’s clothing, bought these garments from a KMF outlet, had copies thereof produced abroad and afterwards started selling those copies in stores in Ireland in 2006.

The Council Regulation n° 6/2002 on community designs (hereinafter the “Regulation”)provides for intellectual property protection via an unregistered community design. This protection relates to the appearance of the whole or a part of a product and has a duration of 3 years as from the date the design was first made available to the public within the Community. Only designs that are new and that show individual character are eligible for this protection. No other formalities need to be fulfilled. This unregistered design right grants its owner the exclusive right to use the design and to prevent any unauthorized third party from using the same, when the contested use results from copying the design.

PROTECTION FOR MEDICINAL PRODUCTS – Recent case-law developments of the Court of Justice of the European Union (December 2013)

Between a patent application for a new medicine, and the marketing authorization for this medicine, a long period of time may occur. This reduces de facto the effective protection conferred by the patent. The European legislator has thus foreseen a mechanism to extend the protection period, called the supplementary protection certificate (hereinafter, ‘SPC’).

This SPC is only valid for the product referred to by the patent, namely the active ingredient or the combination of active ingredients of a medicine, provided that the medicine is covered  by a marketing authorization (hereinafter, MA). Indeed, this extension of the protection cannot be extended to non-patented components, and must be limited to medicines (because it is the time needed to deliver a MA that justifies the extension). The European legislator considered that the holder of both a patent and a certificate should be able to enjoy an overall maximum of 15 years of exclusivity from the time the medicinal product in question first obtains authorization to be put on the market in the Community (Regulation 469/2009 concerning SPC, recital 9).

In practice, this raises sensitive issues of interpretation of regulation 469/2009, which feed an substantial caseload before the Court of Justice of the European Union which is charged with interpreting those texts.

In this context, the CJEU rendered on 12 December 2013 two judgments regarding the issuing of several SPC’s grounded on a single patent and one judgment regarding the concept of “product”.

Read more... pdfProtection_of_medicinal_products_en.pdf

The UPC Agreement is a convention concluded between 25 Member States and which installs a unified patent court. With two regulations adopted by the European Union on 17 December 2012 (the regulations No. 1257/2012 and 1260/2012), this Agreement puts in place a patent which grants unified protection on European level, as well as a common Court which shall have jurisdiction over procedures regarding such patents.

The patent with unitary effect provides its proprietor a unified patent protection in all the Member States participating in the system. The revocation of such patent will also have effect on that whole territory. The primary objective of the new system is to provide the patent holder protection in each of the 25 Member States by means of a single procedure and without the obligation to translate the patent in all national languages.

However, the UPC Agreement does not only concern the patents with unitary effect, as the protection applies as well to ordinary European patents. Moreover, the unified Court shall have jurisdiction over these same ordinary European patents and the applicable law shall be the one contained in the UPC Agreement. During a transitional period, however, undertakings shall have the possibility to choose whether or not being placed under the unified system for the patents of their choice (possibility to “opt-out”).

The concrete implementation of this project shall require at least 13 Member States (of which Germany, England and France) to ratify the UPC Agreement. This being said, companies shall have to evaluate and prepare, from this moment on, certain strategic choices (in particular the question of opt-out). In general, undertakings have to understand the exact scope of this new context in which they shall have to defend their activities and markets, regardless of the fact that they hold patents or not.

The present note shall begin with a summary of the current situation and texts. It shall afterwards clarify the importance of the choices to be made.

More information by reading our full note... pdfUPC_agreement_en.pdf