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EJRR - European Journal of Risk Regulation    Journal TOC RSS feeds Export to Zotero [3 followers]  Follow    
  Full-text available via subscription Subscription journal
     ISSN (Print) 1867-299X
     Published by Lexxion Verlagsgesellschaft Homepage  [12 journals]
  • Book Reviews
    • Abstract: EJRR 1 2013 Book Reviews 113
      Book Reviews
      The Book Reviews section will introduce you to the latest and most interesting books on a
      wide range of topics pertaining to the law and policy of risk regulation. EJRR Book Reviews
      will strive to be present in every edition and will accept reviews from all disciplines. For
      further information on the submission of reviews please contact the Book Reviews Editor at
      david.hornsby@wits.
      PubDate: Thu, 28 Feb 2013 16:53:09 +010
       
  • The HOB-vín Judgment: A Failed Attempt to Standardise the Visual Imagery, Packaging and Appeal ...
    • Abstract: EJRR 1 2013 Case Notes 101
      Case Notes
      The HOB-vín Judgment: A Failed Attempt to Standardise the
      Visual Imagery, Packaging and Appeal of Alcohol Products
      Alberto Alemanno*
      EFTA Court, Case E-2/12, HOB-vín ehf. v. The State Alcohol and Tobacco Company of Iceland
      (ÁTVR)1
      National rules of a EEA State, such as those at stake in the present judgment, under
      which a State monopoly on the retail sale of alcohol, may refuse to accept for sale alcoholic
      beve
      PubDate: Thu, 28 Feb 2013 16:50:36 +010
       
  • Trade, Investment and Risk: Substantial Amendment of the EU Regulatory Framework on Medical ...
    • Abstract: EJRR 1 2013 Reports 97
      ‘illegitimate’ counterfeiters, smugglers and organised
      criminals.” 24 Indeed British America Tobacco
      agreed to pay, under its 2010 cooperation agreement
      with the EU, a sum of 200 million USD over
      a period of 18 years to fund enforcement activities
      against illicit trade.25 This may be a tempting option
      for many governments looking for additional funds,
      notwithstanding the instruction of Article 5.3 of the
      FCTC and correspon
      PubDate: Thu, 28 Feb 2013 16:48:29 +010
       
  • Trade, Investment and Risk: The WHO Protocol to Eliminate Illicit Trade in Tobacco Products: A ...
    • Abstract: EJRR 1 2013 Reports 91
      The WHO Protocol to Eliminate Illicit
      Trade in Tobacco Products:
      A Next Step in International Control of
      Tobacco Products
      Lukasz Gruszczynski*
      This report discusses the main provisions of the recently
      adopted WHO Protocol to Eliminate Illicit Trade in
      Tobacco Products. While recognizing the remarkable
      achievement of the global community in its efforts to
      curb illicit trade in tobacco products at the international
      level
      PubDate: Thu, 28 Feb 2013 16:46:17 +010
       
  • Trade, Investment and Risk: Issues Arising from the European Commission’s Proposal on Biofuels
    • Abstract: EJRR 1 2013 Reports 87
      * Senior Associate, Fratini Vergano – European Lawyers, Brussels.
      1 Directive 98/70/EC of the European Parliament and of the Council
      of 13 October 1998 relating to the quality of petrol and diesel fuels
      and amending Council Directive 93/12/EEC (OJ L 350, 28.12.1998,
      p. 58), last amended by Commission Directive 2011/63/EU of 1 June
      2011 amending, for the purpose of its adaptation to technical progress,
      Directive 98/70/EC of the European
      PubDate: Thu, 28 Feb 2013 16:38:53 +010
       
  • Regulatory Impact Assessment: “Thence We Came Forth to Rebehold the Stars”: A First ...
    • Abstract: 82 Reports EJRR 1 2013
      (regardless of whether an authorization was granted
      or not), or whether it should withhold data from applications
      that received a negative decision and / or
      from withdrawn dossiers.
      Another challenge will be to implement appropriate
      safeguards to protect patient confidentiality. As
      a patient organization representative stated during
      the 22 November workshop, patients can be highly
      protective of their personal health data and the
      PubDate: Thu, 28 Feb 2013 16:36:12 +010
       
  • Pharmaceuticals: The EU Makes Giant Strides towards the Proactive Publication of Clinical Trial Data
    • Abstract: 80 Reports EJRR 1 2013
      mechanism by which perfluorinated substances are
      transferred from blood to milk is not completely
      known, even though it seems related to the strong
      bound of PFCs to proteins.
      For a recent comprehensive review on perfluorinated
      compounds in food in different countries (i.e.
      UK, Spain, Germany, Canada and Japan), see Picó
      et al.32
      3. Nanomaterials
      Growth of the application of nanotechnology products
      is expected in food
      PubDate: Thu, 28 Feb 2013 16:33:52 +010
       
  • Food: Emerging Food Chemical Contaminants from Industry Pollution
    • Abstract: 76 Reports EJRR 1 2013
      for a service should have the right to be engaged,
      be given choices, and have their opinions heard concerning
      its use.
      In addition to public engagement, measures towards
      increased stakeholder transparency must address
      concerns over the wisdom of “playing God.” If
      scientists or industry are not seen as accountable for
      their actions, intended uses of the technology are not
      put forward, and amateurs are viewed as being able
      PubDate: Thu, 28 Feb 2013 16:31:24 +010
       
  • Biotechnology: Microbial Governance – The Ethical Challenge of Synthetic Biology
    • Abstract: EJRR 1 2013 Reports 73
      Reports
      This part of the EJRR hosts reports in which our correspondents keep readers up to date on the most recent
      developments in different areas of risk regulation. Our aim is to fuel the debate and trigger future research on
      cutting-edge risk subjects. The Reports are organised under different policy sections. Further sections will be
      added at regular intervals. If you are interested in contributing to any of the existing sections, please contac
      PubDate: Thu, 28 Feb 2013 16:26:12 +010
       
  • The Role of the Discount Rate in Cost-Benefit Analysis Between Theory and Practice: A ...
    • Abstract: EJRR 1 2013 The Role of the Discount Rate in Cost-Benefit Analysis 59
      The Role of the Discount Rate in Cost-Benefit
      Analysis Between Theory and Practice:
      A Comparative Survey
      Felice Simonelli*
      This study focuses on the role of the discount rate in cost-benefit analysis (CBA) of regulation,
      providing a systematic investigation into regulatory practice vis-à-vis the existing economic
      theories. In the first part, a quick survey of the main economic literature on
      PubDate: Thu, 28 Feb 2013 16:24:21 +010
       
  • Towards Principles-Based Approaches to Governance of Health-Related Research Using Personal Data
    • Abstract: EJRR 1 2013 Approaches to Governance of Health-Related Research Using Personal Data 43
      Towards Principles-Based Approaches
      to Governance of Health-Related Research
      Using Personal Data
      Graeme Laurie* and Nayha Sethi**
      Technological advances in the quality, availability and linkage potential of health data for
      research make the need to develop robust and effective information governance mechanisms
      more pressing than ever before; they also lead us to question the
      PubDate: Thu, 28 Feb 2013 16:19:29 +010
       
  • Not Entirely Reliable: Private Scientific Organizations and Risk Regulation – The Case of ...
    • Abstract: Not Entirely Reliable:
      Private Scientific Organizations and Risk
      Regulation – The Case of Electromagnetic Fields
      Gabriel Doménech Pascual*
      Private scientific organizations exert a great deal of influence in the regulation of some
      technological risks. The high level of expertise of their members is arguably a good reason
      for them to participate in making and monitoring risk regulations, in order to adjust these
      to scientific progress. Nevertheless, there are
      PubDate: Thu, 28 Feb 2013 16:15:28 +010
       
  • Nudge and the Manipulation of Choice
    • Abstract: EJRR 1 2013 Nudge and the Manipulation of Choice 3
      Nudge and the Manipulation of Choice
      A Framework for the Responsible Use of the Nudge Approach
      to Behaviour Change in Public Policy
      Pelle Guldborg Hansen* and Andreas Maaløe Jespersen**
      In Nudge (2008) Richard Thaler and Cass Sunstein suggested that public policy-makers
      arrange decision-making contexts in ways to promote behaviour change in the interest of
      individual citizens as well as that of society. Howeve
      PubDate: Thu, 28 Feb 2013 16:13:29 +010
       
  • Editorial
    • Abstract: The EJRR starts the year by publishing a set of timely research articles engaging with
      some of the most cutting-edge developments in the area of risk regulation: the normative
      debate surrounding the acceptability of behaviourally-informed regulation, the role
      of expertise in the regulation of electromagnetic fields, the governance of e-Health
      initiatives, and the controversial use of discount rate in Cost-Benefit regulatory analysis.
      At a time in which Harvard Law School
      PubDate: Thu, 28 Feb 2013 16:08:35 +010
       
  • Book Reviews
    • Abstract: EJRR 4 2012 Book Reviews 631
      Book Reviews
      The Book Reviews section will introduce you to the latest and most interesting books on a
      wide range of topics pertaining to the law and policy of risk regulation. EJRR Book Reviews
      will strive to be present in every edition and will accept reviews from all disciplines. For
      further information on the submission of reviews please contact the Book Reviews Editor at
      david.hornsby@wits.
      PubDate: Wed, 12 Dec 2012 13:10:51 +010
       
  • On the Concept of Capacity of Exempted Insurance Institutions: Who’s next'
    • Abstract: EJRR 4 2012 Case Notes 625
      On the Concept of Capacity of Exempted Insurance Institutions:
      Who’s next'
      Vadim Mantrov*
      Case C-82/10, European Commission v Ireland [2011] ECR I-00000
      Article 4 of the First Council Directive 73/239/EEC of 24 July 1973 on the coordination
      of laws, regulations and administrative provisions relating to the taking-up and pursuit
      of the business of direct insurance other than life assurance, as amended and repealed
      by the Solvenc
      PubDate: Wed, 12 Dec 2012 13:06:57 +010
       
  • No more Doubts about the Nature of Unit-Linked Products
    • Abstract: EJRR 4 2012 Case Notes 621
      No more Doubts about the Nature of Unit-Linked Products
      Covadonga Díaz Llavona*
      Judgment of the Court (fi fth Chamber) of 1 March 2012 (reference for preliminary ruling),
      Case C—166/11: Ángel Lorenzo González Alonso v Nationale Nederlanden Vida Cía. de
      Seguros y Reaseguros, S.A.E. (Spain)**
      A contract concluded away from business premises, under which life assurance is offered
      in return for payment of a monthly premium to be inv
      PubDate: Wed, 12 Dec 2012 13:05:17 +010
       
  • Trade, Investment and Risk: Sustainability Requirements for Biofuels in the EU: A New Trade and ...
    • Abstract: EJRR 4 2012 Reports 607
      IV. Costs of Misdiagnosis, Adverse Events,
      and Abuse
      To date, relatively little analysis has been conducted
      regarding the costs of misdiagnosis, adverse drug reactions
      with OTC products, and abuse of OTC products.
      The reason these areas remain unexplored is
      due to the diffi culty of obtaining data. Publicly available
      information on these areas is not suffi ciently
      detailed to attribute these instances to OTC drug use.
      The
      PubDate: Wed, 12 Dec 2012 13:02:18 +010
       
  • Pharmaceuticals: Switching Pharmaceutical Products from Prescription to Over-the-Counter: The ...
    • Abstract: EJRR 4 2012 Reports 601
      Pharmaceuticals
      This section updates readers on the latest developments
      in pharmaceutical law, giving information on
      legislation and case law on various matters (such as
      clinical and pre-clinical trials, drug approval and marketing
      authorisation, the role of regulatory agencies)
      and providing analysis on how and to what extent
      they might affect health and security of the individual
      as well as in industry.
      Switching Pharmac
      PubDate: Wed, 12 Dec 2012 13:00:41 +010
       
  • Food: EU Health Claims Regulation and the Marketing of Functional Foods: A Regulatory Void?
    • Abstract: EJRR 4 2012 Reports 577
      Food
      This section aims at updating readers on the latest
      developments of risk-related aspects of food law at EU
      level, giving information on legislation and case law
      on various matters, such as food safety, new diseases,
      animal health and welfare and food labelling.
      EU Health Claims Regulation and
      the Marketing of Functional Foods:
      A Regulatory Void?1
      Herman Lelieveldt* and Cris Boonen**
      This report evaluates the curr
      PubDate: Wed, 12 Dec 2012 12:51:08 +010
       
 
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