COURT OF APPEAL (CIVIL DIVISION)
ON APPEAL FROM THE HIGH COURT OF JUSTICE CHANCERY DIVISION
INTELLECTUAL PROPERTY
MR TERENCE MOWSCHENSON QC
HC 05 COO736 & HC 05 COO97
Strand, London, WC2A 2LL |
||
B e f o r e :
LORD JUSTICE LONGMORE
and
MR JUSTICE LEWISON
____________________
DONCASTER PHARMACEUTICALS GROUP LTD & ORS |
Appellant |
|
- and - |
||
THE BOLTON PHARMACEUTICAL COMPANY 100 LTD |
Respondent |
____________________
MR ANDREW LYKIARDOPOULOS (instructed by Messrs Bpe Solicitors ) for the Respondent
Hearing dates : 18th January 2006
____________________
Crown Copyright ©
Lord Justice Mummery :
Introduction
Summary judgment: general
Trade mark enforcement and parallel imports
"30. The provisions of Articles 28 and 29 shall not preclude prohibitions on imports ….justified on grounds of …..the protection of industrial and commercial property. Such prohibitions or restrictions shall not, however, constitute a means of arbitrary discrimination or a disguised restriction on trade between Member States."
"12 (1) A registered trade mark is not infringed by the use of the trade mark in relation to goods which have been put on the market in the European Economic Area under the trade mark by the proprietor or with his consent."
The appeals
"ambit of the Ideal-Standard case itself raises important questions about market division within the EU. Here it is apparently arguable that a major purpose of the arrangements was market division and is outside the Ideal-Standard principle."
Trade mark ownership
Spanish transactions: AZ and Teofarma
UK Transactions: AZ and Bolton
" 4.1 … for use solely in connection with the marketing, promotion, sales and distribution of the Product in such Country …"
Legal proceedings
Article 30 defence: Ideal Standard.
The Ideal-Standard case
"34. So, application of a national law which would give the trade-mark owner in the importing State the right to oppose the marketing of products which have been put into circulation in the exporting State by him or with his consent is precluded as contrary to Articles 30 and 36. This principle, known as the exhaustion of rights, applies where the owner of the trade mark in the importing State and the owner of the trade mark in the exporting State are the same or where, even if they are separate persons, they are economically linked. A number of situations are covered: products put into circulation by the same undertaking, by a licensee, by a parent company, by a subsidiary of the same group, or by an exclusive distributor.
35. There are numerous instances in national case-law and Community case-law where the trade mark had been assigned to a subsidiary, or to an exclusive distributor in order to enable those undertakings to protect their national markets against parallel imports by taking advantage of restrictive approaches to the exhaustion of rights in the national laws of some States.
36. Article 30 and 36 [now Articles 28 and 30] defeat such manipulation of trade-mark rights since they preclude national laws which enable the holder of the right to oppose imports.
"whether the same principles apply where the trade mark has been assigned, for one or several Member States only, to an undertaking which has no economic link with the assignor and the assignor opposes the marketing in the State in which he has retained the trade mark, of products to which the trade mark has been affixed by the assignee" (paragraph 40).
"43. That view must be rejected. The consent implicit in any assignment is not the consent required for application of the doctrine of exhaustion of rights. For that, the owner of the right in the importing State must, directly or indirectly, be able to determine the products to which the trade mark may be affixed in the exporting State and to control their quality. That power is lost if, by assignment, control over the trade mark is surrendered to a third party having no economic link with the assignor."
Position of Bolton as claimant/assignee
The judgment below
"19. Following the assignment of the trade mark to Teofarma and to the Claimant by AstraZeneca, the Defendants contend that if there is some economic link between Teofarma and the Claimant and AstraZeneca, the doctrine [of exhaustion of rights] may continue to apply. That may be so, but will depend upon the nature of the economic link. In this case, there is no evidence of any meaningful economic link. There is no evidence to suggest that either Teofarma or the Claimant are part of the group controlled by AstraZeneca or other entity which would satisfy the concept of linkage above. The Defendants relied upon the terms of the agreement of 6th September 2001 to transfer the trade mark to Teofarma and to the Claimant dated 23rd September and, in particular, terms of the agreement providing for termination in the event of failure to pay consideration for the trade mark or in the event of bankruptcy.
20. In relation to the agreement with the Claimant, the Defendants tried to rely upon the definition of "product," the technical information licence and various other provisions of the agreement. None of these provisions came near to fulfilling the requirement of linkage as required to import the doctrine of exhaustion of rights. None of them gave AstraZeneca control over the point of manufacture with the quality of the product which is required.
21. The point taken by the Defendants in order to support an argument that AstraZeneca's link to the products supplied in Spain is based upon a letter dated 3rd March 2003 from the Medicines Control Agency that KALTEN in Spain was manufactured by AstraZeneca Farmaceutica Spain SA. At that time, it is likely that Teofarma was still using products supplied by AstraZeneca. As I have said, the evidence is that AstraZeneca ceased to supply in April 2001, when its supplies had a shelf life of three years. The Spanish agreement makes it plain that Teofarma and AstraZeneca would sever all links by 30th June 2002 at the latest: I refer to clauses 3.1 and 6.1 of that agreement.
22. The packets of the Spanish manufactured product bear Teofarma as the manufacturer in its labelling. The Spanish leaflet inside the packet describes Teofarma as the manufacturer under EC Regulation of Article 59 of Directive 2001/83 as a product such as medicine must bear the name and address of the manufacturer. The only [reference] to AstraZeneca Farmaceutica Spain SA is in a leaflet produced by the Defendants and inserted in the packets for sale in the UK. Indeed, it appears from the Defendants' evidence that they now accept that AstraZeneca is not linked to Teofarma any longer …."
Discussion and conclusion
Result
Lord Justice Longmore:
Mr Justice Lewison: