Gen-Probe Incorporated v Beckman Coulter, Inc
[2022] FCA 194
At a glance
Source factsCourt
Federal Court of Australia
Decision date
2022-03-08
Before
O'Bryan J
Source
Original judgment source is linked above.
Judgment (9 paragraphs)
Introduction 1 This proceeding concerns International Registration 1370198 with the World Intellectual Property Organisation (WIPO) of the trade mark OPEN ACCESS in classes 1, 5, 9 and 10 held by the appellant (Gen-Probe) and Gen-Probe's request, under Art 3ter(1) of the Protocol Relating to the Madrid Agreement Concerning the International Registration of Marks (27 June 1989) (Madrid Protocol), for extension to Australia of the protection resulting from the international registration (such request being International Registration Designating Australia 1880980 (the IRDA)). The goods in respect of which protection was sought were as follows: Class 1: Nucleic acids, chemical reagents and buffers for use with automated in vitro diagnostic specimen analyzer instruments for detection and assay of nucleic acids for research use; cartridges and containers sold prefilled primarily with lyophilized and liquid reagents for detection and assay of nucleic acids for research use primarily directed to laboratories for use by laboratory technicians Class 5: Nucleic acids, chemical reagents and buffers for use with automated in vitro diagnostic specimen analyzer instruments for detection and assay of nucleic acids for medical diagnostic use; cartridges and containers sold prefilled primarily with lyophilized and liquid reagents for detection and assay of nucleic acids for medical diagnostic use primarily directed to laboratories for use by laboratory technicians Class 9: Automated in vitro diagnostic specimen analyzer instrument and parts thereof, for the detection and assay of nucleic acids, all for laboratory use; computer software for the organization and analysis of specimen test data and to configure and control the operation of instrument system for in vitro diagnostic specimen analysis; none of the foregoing measuring electrical resistance Class 10: Automated in vitro diagnostic specimen analyzer instrument and parts thereof, for the detection and assay of nucleic acids, all for medical diagnostic use; none of the foregoing measuring electrical resistance 2 Section 189A of the Trade Marks Act 1995 (Cth) (TM Act) provides that regulations made under the Act may provide for such matters as are necessary to enable the performance of Australia's obligations under the Madrid Protocol. Those regulations are in Pt 17A of the Trade Marks Regulations 1995 (Cth) (TM Regulations) titled "Protected International Trade Marks under the Madrid Protocol". 3 Gen-Probe filed its International Registration pursuant to Art 2 of the Madrid Protocol on 30 August 2017. The International Registration was based on United States Trade Mark Application No. 87360259, which claims a priority date of 6 March 2017. Gen-Probe requested extension of protection of its International Registration to Australia and, on 19 October 2017, IP Australia received notification of that International Registration from WIPO. 4 On 18 December 2019, a delegate of the Registrar of Trade Marks (Registrar) refused extension to Australia of protection resulting from the International Registration: Beckman Coulter, Inc v Gen-Probe Incorporated [2019] ATMO 182. The delegate decided that the respondent (BCI) had established a ground of opposition under s 60 of the TM Act on the basis of the reputation of its registered Australian trade marks for ACCESS (registration numbers 571344, 571345 and 571346). 5 By notice of appeal dated 28 January 2020, Gen-Probe appealed from the decision of the Registrar pursuant to s 56 of the TM Act and reg 17A.34P of the TM Regulations. 6 By notice of contention dated 20 March 2020, BCI advanced contentions that the delegate's decision should be affirmed on additional grounds, specifically s 44 of the TM Act (on the basis that the OPEN ACCESS trade mark is substantially identical with, or deceptively similar to, BCI's ACCESS trade marks) and s 42(b) of the TM Act (on the basis that the use of the OPEN ACCESS trade mark would be contrary to ss 18 and 29 of the Australian Consumer Law, being Sch 2 to the Competition and Consumer Act 2010 (Cth), again by reason of BCI's ACCESS trade marks). 7 On 12 October 2020, Gen-Probe applied to the Registrar under s 92 of the TM Act to remove BCI's ACCESS trade marks from the Register for non-use. On 15 January 2021, a delegate of the Registrar referred the non-use applications to this Court pursuant to s 94 of the TM Act. On 5 February 2021, I made orders that the non-use applications be heard and determined by this Court as part of the appeal proceeding. On 16 February 2021, Gen-Probe filed an interlocutory application seeking an order directing the Registrar to rectify the Register by removing, or otherwise narrowing the specifications of, BCI's ACCESS trade marks on the ground of non-use under s 101(2) of the TM Act. 8 The appeal and non-use application were heard by me during May 2021 and I reserved my decision on 11 May 2021. 9 On 9 December 2021, the parties informed the Court they were in advanced settlement discussions regarding the matters at issue in the proceeding and were optimistic that a settlement would be reached pursuant to which the parties would propose consent orders to resolve the proceeding. 10 Ultimately, on 24 February 2022, the parties informed the Court that an agreement had been reached to resolve the proceeding and provided the Court with proposed consent orders. The proposed orders were as follows: (a) Gen-Probe's appeal is allowed. (b) The decision of the Registrar refusing to extend protection to Gen-Probe's IRDA for the trade mark OPEN ACCESS is set aside. (c) The Registrar is directed to extend protection of Gen-Probe's IRDA in respect of the goods and services set out in the schedule to the proposed orders. (d) Gen-Probe's interlocutory application filed on 16 February 2021 is dismissed with no order as to costs. (e) The Registrar is directed to withdraw Gen-Probe's non-use removal proceedings against BCI's Australian trade mark registrations nos. 571344, 571345 and 571346, with no direction as to costs. (f) The proceedings are discontinued with no order as to costs. 11 The goods set out in the schedule to the proposed orders comprise a narrower specification than in the IRDA and were as follows (with changes to the IRDA specification marked): Class 1: Nucleic acids, chemical reagents and buffers for use with in automated in vitro diagnostic specimen analyzer instruments for performing nucleic acid amplification reactions for the detection and assay of nucleic acids for research use; cartridges and containers sold prefilled primarily with lyophilized and liquid reagents for performing nucleic acid amplification reactions for the detection and assay of nucleic acids for research use primarily directed to laboratories for use by laboratory technicians Class 5: Nucleic acids, chemical reagents and buffers for use with in automated in vitro diagnostic specimen analyzer instruments for performing nucleic acid amplification reactions for the detection and assay of nucleic acids for medical diagnostic use in connection with laboratory developed tests; cartridges and containers sold prefilled primarily with lyophilized and liquid reagents for performing nucleic acid amplification reactions for the detection and assay of nucleic acids for medical diagnostic use in connection with laboratory developed tests primarily directed to laboratories for use by laboratory technicians Class 9: Parts for automated Automated in vitro diagnostic specimen analyzer instrument for performing nucleic acid amplification reactions, and parts thereof, for the detection and assay of nucleic acids, all for laboratory use in connection with laboratory developed tests; computer software for the organization and analysis of specimen test data in connection with laboratory developed tests and to configure and control the operation of instrument system for performing in vitro nucleic acid amplification reactions for diagnostic specimen analysis; none of the foregoing measuring electrical resistance Class 10: Parts for automated Automated in vitro diagnostic specimen analyzer instrument for performing nucleic acid amplification reactions, and parts thereof, for the detection and assay of nucleic acids, all for medical diagnostic use in connection with laboratory developed tests; none of the foregoing measuring electrical resistance 12 The Court requested the parties to file submissions in support of those orders addressing, in particular, the power of the Court to make the orders sought by consent. Those submissions were filed on 4 March 2022. 13 The submissions said very little about the factual basis on which the parties requested the Court to make orders in the proceeding. Nevertheless, the Court understands from the submissions that, by agreement between the parties: (a) BCI wishes to withdraw its opposition to Gen-Probe's IRDA; (b) Gen-Probe requests an amendment to the specification of goods and services listed in the IRDA; and (c) Gen-Probe seeks the dismissal of its interlocutory application concerning removal of the BCI ACCESS trade marks for non-use and wishes to withdraw the underlying application made to the Registrar. 14 For the reasons set out below, I am satisfied that the orders generally as sought by the parties by consent are within power and are appropriate to be made (subject to certain amendments noted below).