Astra/Zeneca AB

Case [2007] ADO 4


DESIGNS ACT 2003


DECISION OF A DEPUTY REGISTRAR OF DESIGNS

Re:      Design 303092 in the name of AstraZeneca AB

Background

I heard the owner today regarding the issue of whether the design was distinctive having regard to the prior art - Swedish Design 77534.

At the outset of the hearing, I indicated that I had some familiarity with products of this nature, with a daughter and granddaughter both using such devices in association with asthma treatment. In that context I indicated that I had a view that a user would consider a device that indicated the number of puffs remaining would be of great significance to users, and accordingly such a user would give attention to the region of the device containing the indication.

However, I expressed concern that this interest was associated with the function provided by the indicator, and not the appearance of the indicator per se. In particular, I hypothesized that if the marks indicative of the scale were purely printing on the surface (with no underlying functionality), the user would have a quite different view of the product. Accordingly I was concerned to ensure that the Design was assessed on the basis of its visual features - and the fact that the utility of the design only arose as a result of the functional elements that were not part of the design (nor shown in the Design). Relating to this, I was concerned about the extent to which the standard of the informed user should be impacted by the elements of functionality.

Following discussion of the statutory and factual issues relating to these concerns, (including issues of the Trade Practices Act if a functional indicator did not exist) I am of the view that:

  1. The relevant approach is to assess the standard of the informed user as of the priority date;
  1. If the informed user's assessment is affected by an expectation of functionality, the fact that such functionality may not actually exist is not relevant. In this case, the question is: would the informed user's attention be drawn to the indicator on the end?  If the user would look there in the expectation that there is a useful indicator present, that is sufficient. In particular, it does not matter whether or not the indicator would function. If the user's attention is particularly drawn to that feature, that fact alone is sufficient to indicate the feature as being one of importance (in the Designs context).
  1. In this case the owner has provided several declarations from relevant users that indicate their attention would be drawn to this feature. My own assessment similarly is that users' attention would be drawn to the feature - because of its potential functionality. Accordingly, in the context of s.19(2)(b), and applying the standard of an informed user, this feature would have greater relative importance with respect to the remaining parts of the design than would otherwise be the case..
  1. On this basis, I am satisfied that the overall impression of this product is clearly distinctive from the cited prior art (which is exactly the same apart from the indicator).
  1. Late in the prosecution, the owner filed a request to amend - to add a Statement of Newness and Distinctiveness. Apart from certain statutory difficulties concerning the allowability of that amendment, the owner indicated they did not wish to proceed with that amendment.

Conclusion

I am satisfied that the present design is new and distinctive compared to the cited prior art. Accordingly I direct that - upon the owner filing a formal withdrawal of the proposed amendments - examination of this design be taken as 'completed' pursuant to s.65(3), and that the provisions of s.67 now apply.

D Herald
Deputy Registrar of Designs
5 June 2007

Details
AGLC
Astra/Zeneca AB [2007] ADO 4
Case
[2007] ADO 4
Decision Date

CaseChat Overview and Summary

The decision concerns the distinctiveness of a design in the name of AstraZeneca AB, as per Design 303092. The Deputy Registrar of Designs was tasked with determining whether the design was distinctive in light of prior art, specifically Swedish Design 77534. The Deputy Registrar held a hearing to assess the distinctiveness of the design based on the standard of the informed user, considering whether the design's features were visually significant, regardless of any functional aspects.

The central legal issue was whether the design, which included an indicator of the number of puffs remaining on an inhaler, was distinctive compared to the prior art. The Deputy Registrar considered the extent to which the informed user's perception of distinctiveness was influenced by the potential functionality of the design features. The Deputy Registrar concluded that the informed user's attention would be drawn to the indicator due to its potential functionality, which would render it a feature of significant importance in assessing the overall distinctiveness of the design.

The Deputy Registrar reasoned that the standard of the informed user should be applied as of the priority date and that the user's expectation of functionality, regardless of its actual existence, would affect their assessment. The Deputy Registrar was satisfied that the design's overall impression was distinctive from the prior art due to the indicator. The Deputy Registrar further noted that the owner had provided declarations from relevant users indicating their attention would be drawn to the indicator. Consequently, the Deputy Registrar determined that the design was new and distinctive.

The Deputy Registrar directed that upon the owner filing a formal withdrawal of the proposed amendments, the examination of the design be taken as completed, and that the provisions of section 67 of the Designs Act 2003 now apply. This decision underscores the importance of user perception and functionality in assessing the distinctiveness of a design.

Orders

Orders of the court

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Background

Background to the litigation

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Evidence

Evidence Before The Court

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Decision

Reasons for decision

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Ratio Decidendi

Legal Principle Established

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