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Abuse of Economic Dependence - The Centre for European Policy ...

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<strong>The</strong> Gap in the Application <strong>of</strong> Article 82 65<br />

A Commission’s case which can be identified as a ‘gap’ case 61 is Bayer<br />

(Adalat). 62 Owing to wide price differentials <strong>for</strong> the product between Spain<br />

and France on the one hand and the United Kingdom on the other, there<br />

was a surge in parallel trade. In response, Bayer began to restrict supplies<br />

to its Spanish and French distributors with the goal <strong>of</strong> allowing them sufficient<br />

stock only <strong>for</strong> their national markets. Although distributors were still<br />

entitled to export the stock which they received, the reduced supplies taken<br />

together with the distributors’ obligations to supply the national market<br />

reduced the scope <strong>for</strong> parallel exports.<br />

This case concerned Adalat, a product belonging to a category <strong>of</strong> medicinal<br />

products known as calcium antagonists, suitable <strong>for</strong> treating certain<br />

cardiovascular diseases (coronary heart disease, arterial hypertension and<br />

congestive heart failure). <strong>The</strong> scope <strong>of</strong> the decision was limited to two products<br />

in the Adalat range, namely the 10 mg capsule (marketed in the United<br />

Kingdom and Spain under the name Adalat and in France under the name<br />

Adalate) and the 20 mg modified-release tablet (marketed in the United<br />

Kingdom and Spain under the name Adalat-Retard and in France under the<br />

name Adalate 20 mg LP).<br />

As regards the geographical market, the Commission held that the relevant<br />

markets in this case were the national markets, taking account <strong>of</strong> the<br />

fact that the business <strong>of</strong> the pharmaceutical industry took place in an essentially<br />

national context, marketing authorization <strong>for</strong> a medicinal product<br />

falling exclusively within the competence <strong>of</strong> the Member States. Moreover,<br />

the sale <strong>of</strong> medicines was influenced by the administrative, and particularly<br />

the purchase policies adopted in Member States, especially in France and<br />

Spain, where prices were directly set by the competent national authority.<br />

Finally, the Commission argued that differences in price-fixing methods and<br />

refund arrangements meant that there were wide disparities in the prices <strong>of</strong><br />

medicinal products in Member States.<br />

As regards the product market, the Commission argued that it is defined<br />

by reference to the criterion <strong>of</strong> identical therapeutic uses <strong>for</strong> the various<br />

competing products. <strong>The</strong> relevant market was defined as follows:<br />

• Primarily, as far as coronary heart disease and hypertension were<br />

concerned, the United Kingdom was deemed to be the major relevant<br />

61 <strong>The</strong> Commission does not publish detailed decisions where it states that an abuse has not<br />

been substantiated. Although following Regulation 1/2003, the Commission can publish such<br />

decisions.<br />

62 Commission Decision 96/478 Adalat [1996] OJ L201/1 (January 10, 1996); Case T-<br />

41/96 R Bayer AG v Commission [1996] ECR II-381 (Order <strong>of</strong> June 3, 1996), [2000] ECR II-<br />

3383 (Judgment <strong>of</strong> October 26, 2000); Joined Cases C-2/01 P and C-3/01 P Bundesverband<br />

der Arzneimittel-Importeure eV and Commission v Bayer AG (Advocate General Opinion <strong>of</strong><br />

May 22, 2003, ECJ Judgment <strong>of</strong> January 6, 2004).

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