IP Law, Raising the Bar and Non-pharmaceuticals
The Intellectual Property Laws Amendment (Raising the Bar) Act 2012 received Royal Assent on Sunday 15 April 2012, and is a major reform of thePatents Act 1990. Most of the provisions will take effect from 16 April 2013. However the exemptions to infringement for experimental purposes and for the regulatory approval of non-pharmaceutical products take immediate effect, and became law on 16 April 2012. The aim of these infringement exemptions is to encourage follow-on innovation.
Acts for obtaining regulatory approval (non-pharmaceuticals)
There are existing infringement exemptions in place for the acts involved in obtaining regulatory approval of pharmaceuticals. The amendments in the Intellectual Property Laws Amendment (Raising the Bar) Act 2012 introduce a similar exemption from infringement for non-pharmaceutical products that are legally required to undergo regulatory approval in Australia or other countries. This exemption became law on the Monday 16 April 2012 and it exempts regulatory approval activities done, on or after that date.
Other products that are required to undergo regulatory approval before they can be marketed in Australia include medical devices through the Therapeutic Goods Administration (TGA), agricultural and veterinary chemical products through the Australian Pesticides and Veterinary Medicines Authority (APVMA) and industrial chemicals through the National Industrial Chemicals Notification and Assessment Scheme (NICNAS). Previously a regulatory approval process could not be undertaken in Australia for generic products of these types until the innovator patent had expired. As a consequence entry of competitor products onto the market was postponed and which effectively provide patent holders with an extension of their patent term, which ranged from weeks to years.
The extension of the infringement exemption from pharmaceutical products to non-pharmaceuticals is in line with provisions in place in New Zealand, Israel and Canada. It is in contrast with the corresponding provisions in Europe and the US which currently only have exemptions for regulatory approval of medicines for human and veterinary use.
The infringement exemption will allow companies to perform research and development within Australia which is needed to obtain regulatory approval both within Australia and overseas. This is expected to reduce the need to conduct research and development overseas. The Australian Government proposes that this will allow Australian companies to compete with overseas competitors, which tend to enter foreign markets more quickly after the expiration of a patent than Australian companies.
It is worth noting that these exemptions are intended solely for the processes of obtaining regulatory approval and are not for other purposes. For example, they are not intended to allow, in the process of seeking regulatory approval, stockpiling of a patented product for sale upon expiry of the patent, or manufacture of the product for export to another country.
Acts for experimental purposes
Previously there were no statutory provisions clarifying the extent to which researchers could conduct experiments without infringing a patent. It was widely assumed that a common law experimental use exemption existed within the patent system but there was uncertainty as to the scope of the exemptions. This uncertainty was thought to have a knock-on effect on the efficiency of research and that it may discourage innovation due to the time, energy and cost involved in assessing freedom to operate before commencing research.
The exemptions introduced by the Intellectual Property Laws Amendment (Raising the Bar) Act 2012 attempt to balance the commercial interests of applicants and the freedom of researchers to conduct experiments without being subject to patent infringement proceedings.
The Intellectual Property Laws Amendment (Raising the Bar) Act 2012 introduces an exemption from infringement for the use of the patented invention for experimental purposes. The exemption became law on 16 April and exempts experimental activities done, on or after that date. The amendment states that:
The amendment includes the following list of experimental purposes which would be exempt from infringement:
However, this list is not intended to be limiting and it is open for a court to find that other activities fall within the meaning of â€œexperimentalâ€.
This approach is consistent with the system currently in place in Europe. It also aligns Australia with the UK, New Zealand, Japan, Germany, Switzerland and Belgium which either currently have research exemptions or are in the process of implementing similar provisions. The exemption is broader than the common law exemption that currently exists in the US.
It is worth highlighting that these infringement exemptions can also apply in a commercial setting. For example, infringement exemption would also apply to the following situations where:
The acts performed on or after 16 April 2012 are exempt from infringement if they are predominantly undertaken for the purpose of gaining new knowledge or testing a principle or hypothesis about the invention. Hence, if the research is conducted solely to improve a patented invention the activity would still be exempt, even if it was intended to commercialise the improvement.
However, it is not intended that these provisions will exempt the use of â€œresearch toolsâ€ from infringement. For example, the use of a patented assay to facilitate the discovery of active compounds will still be an infringement, as the assay is being used as a tool and the experiments do not relate to the assay itself.
The general consensus is that these research exemptions are a welcomed clarification to the research community on their freedom to operate and also to patent holders as to the circumstances in which they can enforce their patent rights. The Australian Government expects that these exemptions will encourage follow-on innovation and increase the access to new technologies.
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