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Protecting Public and Planet: Environmental and Health Regulation in the United States and the European Union

Protecting Public and Planet: Environmental and Health Regulation in the United States and the European Union. Mitchell P. Smith The University of Oklahoma. Environmental and Health Regulation. chemicals. Environmental and Health Regulation. autos recycling.

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Protecting Public and Planet: Environmental and Health Regulation in the United States and the European Union

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  1. Protecting Public and Planet: Environmental and Health Regulation in the United States and the European Union Mitchell P. Smith The University of Oklahoma

  2. Environmental and Health Regulation chemicals

  3. Environmental and Health Regulation autos recycling

  4. Environmental and Health Regulation health claims

  5. The United States:Environmental and Health Regulation in the 21st century Rigor of Regulation Time

  6. The European Union:Environmental and Health Regulation in the 21st century Rigor of Regulation Time

  7. The U.S. and the EUDiverging Trajectories Rigor of Regulation EU U.S. Time

  8. Diverging U.S. and EU Trajectories WHY?

  9. Explaining Diverging U.S. and EU Trajectories Culture?

  10. Europe: Precaution and Cultural Aversion to Risk • BSE (“mad cow” disease) • dioxin in beverages, poultry, eggs (1999) • preference for “traditional” foods (no GMOs)

  11. Evidence Against Cultural Argument:The U.S. • high level of precaution displayed in past regulatory policy (health claims on food labels) • policy toward tobacco consumption • restrictions on blood donations from people exposed to BSE beef • regulation of nitrogen oxides from diesel vehicles

  12. Explaining Diverging U.S. and EU Trajectories State-Market balance?

  13. State-Market Balance ArgumentAmerican liberal capitalism vs. state-centered European dirigisme • Political economy of US => regulatory structures give primacy to free competition • Europe’s coordinated capitalism => constrains market exchange in favor of public goods

  14. State-Market Balance ExplanationArguments Against • European market has favored intensification of market competition • EU concern with regulatory burden on industry (regulatory impact assessment) • Policy discourse over regulation in EU closely resembles that in the U.S.

  15. Court Decisions? • U.S. courts => high evidentiary standards (on FDA, e.g.) free commercial speech • ECJ => follows this pattern free commercial speech, proportionality

  16. Industry Lobbying?

  17. Industry Lobbying?power of industry lobby in U.S. • organizational resources • access to policy making

  18. Industry Lobbying?power of industry lobby in U.S. . . and relatively greater access of environmental interest associations in the EU

  19. Industry Lobbying?No • U.S.=> court decisions have trumped lobbying • EU => rising industry access

  20. Rising Industry Access in the EU • increased legislative powers of EP => more industry resources invested in lobbying • access via Internal Market Committee (2004; 6th EP) and political groups • Competitiveness Council (2002)

  21. What then? If not cultural attitudes toward risk, national political economies, court decisions, or industry lobbying? Rigor of Regulation EU U.S. Time

  22. Institutions and Regulatory Tradeoffs The Regulatory Dilemma in the US: competitiveness regulatory objectives vs. The EU’s Regulatory Trilemma:

  23. The Regulatory Dilemma in the U.S. Outcomes include: • Voluntary regulation (TRI) • Regulatory “preemption” competitiveness regulatory objectives

  24. The EU’s Regulatory Trilemma EU Regulation: • Harmonizes standards • Intensifies cross-border exchange • Fosters interest articulation at EU level

  25. Implications of Court Decisions • In U.S., court decisions constrain federal regulatory ambitions • In the EU, court decisions define areas where single market regulation is incomplete

  26. Illustrating the Argument: health claims Case demonstrates: (1) history of precaution in U.S. (2) contrasting role of court decisions (3) rising industry lobby in EU

  27. US Regulatory Regime • 1906-mid 1980s: health claims as implied drug claims (hence no claims) • In 1990 industry lobbying leads to Nutrition Labeling and Education Act (effective 1993 and largely a response to diffuse actions by states) • No preemption by states • “significant scientific agreement” standard • 1993: only 7 claims permitted; 5 more by 2001

  28. US Regulatory Regime Landmark 1999 court case: Pearson v. Shalala • Proportionality • Free commercial speech • Note parallel to ECJ rulings in early 2000s (which similarly struck down national laws regulating health claims on the grounds that they were excessively restrictive and disproportionate to the objectives sought).

  29. US Regulatory Regime post-Pearson v. Shalala FDA endeavors to sustain its regulatory approach to health claims on foods

  30. US Regulatory Regime Subsequent court cases in 2000s (e.g., Whitaker v Thompson I, 2002): • FDA too restrictive • Has FDA considered all available evidence? • Why not a disclaimer? • “qualified claims” based on “credible scientific evidence” or “some scientific evidence” • Welter of claims (first approved claim July 2003: unsaturated fats in tree nuts => reduced risk of heart disease) • Yet FDA continues to exercise enforcement discretion

  31. US Regulatory Regime By 2010, following Alliance for Natural Health vSebelius: • Burden on FDA • Minimally restrictive disclaimers • Show disclaimer would confuse consumers

  32. US Regulatory Regime Distinction between rules for dietary supplements and rules for foods breaks down =

  33. US Regulatory Regime:The Result

  34. EU Regulatory Regime Wide variation through 1990s: • Austria highly restrictive • Voluntary codes in Sweden and UK • Case by case approach in Germany and France

  35. EU Regulatory Regime ECJ decisions in early 2000s: • 1975 Austrian LMG (2003) • DouweEgberts (2004) • Parallel to U.S. decisions: proportionality • Similar impact on national regulatory regime

  36. EU Regulatory Regime However, institutional dynamics differ from US: • Business sector wants legal certainty (as in U.S.) • European Commission: barrier to free movement of foodstuffs • DG SANCO: barrier to high level of consumer & public health protection • National health ministers want to reclaim regulatory control

  37. EU Regulatory Regime: The Result 2003 Commission proposal: • Disease reduction claims subject to EFSA approval • Nutrition profiles

  38. EU Regulatory Regime: The Result • Industry lobbying: impact on innovation and competitiveness • EP cuts nutrition profiles in first reading • National health ministers restore nutrition profiles • Regulation on Nutrition and Health Claims on Foods enters into force January 2007

  39. European Parliament Second Reading Debate • ”. . . the tenacious lobby of food and particularly the drinks industry has not been as effective this time around;” could the EP second reading vote be attributed to the fact that "Members are simply embarrassed . . . that for once, the Council was more progressive than Parliament?” -- Dutch MEP Kartika Tamara Liotard, European United Left • ”. . . we have nothing to gain from European law being drafted at the International Sweets and Biscuits Fair in Cologne.” -- FrédériqueRies, French Liberal Democrat MEP

  40. EU Regulatory Regime: The Result Industry lobbying continues: • More than 44,000 proposed claims submitted to Commission and forwarded to EFSA by Jan. 1, 2008 • EP seeks to remove nutrition profiles in 2010 • Committee passes this amendment; tie vote (309-309) in plenary

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