Why this blog?

There are many companies supplying agricultural and veterinary chemicals in Australia. Their ability to operate in the Australian market, and the ability of larger companies to operate in the market, is dependent on a dysfunctional regulatory system. Industry associations and individuals have been arguing the regulatory system needs to be improved for some time. The Government appears to be listening and changes are being proposed. This blog is designed to provide a forum for debating the changes, offering suggestions and comments and becoming informed.

To ensure changes are “palatable”, it is necessary to participate in the reform process. Most companies are not participating. Most are relatively small — 92% of companies are considered to be small in terms of sales of agricultural and veterinary chemicals in Australia. These small companies account for only 14% of total agvet chemical sales in Australia. The majority of these companies do not have in-house regulatory expertise. They do not have time to become involved in preparing responses to government proposals to reform the regulatory system – but their survival often depends on the regulatory system that allows them to participate in the market, to develop new products, and to grow their business.

Most companies in the Australian agricultural and veterinary chemical industry are not members of any industry association. Remaining fully informed about the regulatory system is difficult and smaller companies have little time to comment on proposed changes. Many companies can feel alone, thinking they are the only ones having problems with the regulatory process in Australia.

The best way to ensure you are fully informed is to be an active member of a relevant industry association. This site contains links to relevant industry associations including ACCORD, Australasian Compliance Institute, CropLife Australia and PACIA.

Maybe you are a member of an industry association. Maybe you are not. Irrespective, the changes proposed in the policy discussion paper are important. They deserve open discussion and debate. The discussion document is available at: http://www.daff.gov.au/agriculture-food/food/regulation-safety/ag-vet-chemicals/better-regulation-of-ag-vet-chemicals.

In the past, I have responded to earlier proposals by involvement in a working group. I have chaired a number of working groups for the Australasian Compliance Institute. This time, with the discussion paper being released in November with responses originally due in January, a time when most businesses slow down and people take holidays, it was determined we would have difficulty in convening a working group. I therefore prepared a response and submitted it personally (see my submission in the “Shared Documents” tab).

The document I prepared contains my views. This blog gives others an opportunity for everybody to comment in a public forum. It allows debate on topics and issues.

The objective of this blog is to foster public discussion about regulation of agricultural and veterinary chemicals in Australia; to bring the issues of concern into the open and to debate ways to address those issues. The ultimate objective is to provide a forum for people, whether members of industry associations or not, to contribute to the debate and help ensure we get a regulatory system that we can live with.

While this is an open forum, there are some rules for participation:

• Anybody can read the posts and comments. However, this is a forum for exchange of information and debate. The views expressed are not necessarily those of N&F Pty Ltd. N&F Pty Ltd does not and cannot warrant the accuracy of any statements, views or comments expressed on this site. Before relying upon any statements, advice or suggestions, you should check the accuracy/relevance/applicability of such statements, advice or suggestions to your specific situation.
• To leave comments, you need to register. We require some personal details to reduce the possibility of comments being inappropriately generated. The personal details will not be shared or sold. They will not be disclosed to APVMA or any other third party. Your comments will appear under the pseudonym you choose during registration.
• All comments will be moderated before they are made public. Comments that are defamatory, obscene or contain commercial messages will be edited or deleted. Comments should not perpetuate rumours about APVMA, any company, organisation or individual.
• Similarly, mass postings, including where a large number of people attempt to post the same comment, will be edited. We will publish the first comment and state that a large number of similar comments were received.

I hope this blog will be useful. The only way for it to achieve its objectives is for people to comment – whether you agree or disagree. I invite you to raise issues not raised by others, to give examples, to provide suggestions and comments. If preferred, feel free to contact me (Mike Tichon) at:

Telephone (office): +61 (0)2 8861 5000
Telephone (mobile): +61 (0)422 300 747
Email: mike.tichon@competitive-advantage.com.au

Michael Tichon

After more than 20 years working in developing, registering and commercialising chemicals globally, Michael Tichon returned to Australia from the USA in 2002 to establish Competitive Advantage (trading name for N&F Pty Ltd) to help organisations in regulated industries (especially chemicals) get their products onto the market and keep them on the market.

Competitive Advantage helps organisations obtain approvals and registrations for their products in Australia, New Zealand and elsewhere. Competitive Advantage concentrates on agricultural and veterinary chemicals and food chemicals. An associated company (Cintox) deals with other chemicals including industrial and consumer chemicals, cosmetics, disinfectants, etc.

Mr Tichon was transferred to the USA as global head of regulatory for the agricultural and public health products division of a Fortune 500 pharmaceutical company in 1997. Prior to moving to the USA he was head of product development and registration of that company’s agricultural and public health products throughout the Asia Pacific Region.

With the sale of the agricultural and public health products business, Mr Tichon transferred as global head of regulatory and QA to the new entity formed by the acquisition.

Earlier in his career Mr Tichon was national product development manager, head of the animal health products business and national marketing manager for agricultural products for a major agrochemical company operating in Australia as well as having worked as product manager for agricultural and pasture/animal feed products for that company’s affiliate in the UK.

Originally trained as ecologist/entomologist, Mr Tichon has a particular interest in new technologies and in the risks posed by chemicals in the environment (including humans within the environment). He has been a member of various industry task forces/working groups to address issues, including those related to developing technologies.

Michael Tichon can be contacted at:

Email: mike.tichon@competitive-advantage.com.au.
Telephone (office): +61 (0)2 8861 5000
Telephone (mobile): +61 (0)422 300 747

Regulation of Agricultural and Veterinary Chemicals in Australia

The regulatory system that controls agricultural and veterinary chemicals in Australia is dysfunctional. Registration of new products takes too long, registration of new products costs too much, data requirements are excessive and the approach to regulation is overly conservative. Changes to the regulation of agricultural and veterinary chemicals have now been proposed by the Government. However, caution is required in implementing some of the proposals. We need to ensure that useful products are not lost because re-registration is too expensive. We need to ensure that products available for use in other countries are not prevented from being available because of an overly expensive and overly conservative regulatory system.

In November 2010 the Minister of Agriculture, Fisheries and Forestry, Senator the Hon. Joe Ludwig released a discussion paper titled “Better Regulation of Agricultural and Veterinary Chemicals”.  In his forward, the Minister stated, “The Australian Government recognises the system is not working as effectively as it should and is looking at options for reform, to better protect human health and the environment; and increase the authority’s efficiency and effectiveness”.

What is proposed in this document and will the proposed reforms improve the regulation of agricultural and veterinary chemcials?

1.      Implementing a risk framework for agricultural and veterinary chemicals.  The Agricultural and Veterinary Chemicals Code Act 1994 requires APVMA to register a product unless APVMA is not satisfied the product will not pose an undue hazard to people, animals, the environment and trade.  What is an “undue hazard”?  APVMA’s approach to this questions is to publish a long list of information in its guidelines and require applicants address everything on that list, whether relevant to the specific application or not.  By asking for unnecessary information APVMA not only delays registration but frequently imposes significant additional costs.  The regulated community needs to understand the risks APVMA is concerned about, propose how to mitigate those risks and, when mitigation proposals are accepted, be required to implement and maintain those mitigation measures — not show they can generate all the information, whether relevant or not, listed in the APVMA website.

2.      Improving the quality and efficiency of assessments and registration. I have argued for a long time that Screening of applications is a complex, registration delaying process.  The Australasian Compliance Institute met with the then Minister of Finance Lindsay Tanner and outlined a number of problems.  Screening was one issue, giving the example of an application submitted to APVMA which, at the time of the meeting, was still in Screening.  The same product took a few weeks to clear Screening when submitted to the US EPA.  There are stories of applications for which the Evaluation timeframe stated in the Regulations was 3 months taking significantly longer to complete Screening.  Why?  These same products are registered in other countries.   Is the regulator more concerned with process or outcomes?

3.      Using overseas assessments to their full extent. Australia, with 2-3% of the global market for agricultural chemicals, is a small market.  We cannot afford to have a regulatory system that considers the regulatory process in other advanced countries incompetent.  These regulatory authorities that apparently do not do an adequate job in assessing products are the same ones that have completed reviews of chemicals and found some products to be no longer suitable for use.  Eventually — after media pressure — APVMA concludes that the regulatory decisions by these same overseas regulators were correct and bans were appropriate, as in the case of endosulfan. Are the decisions being made by the media, by overseas regulators or APVMA? If APVMA is coming to the same scientific conclusions as the overseas regulators why is it necessary for APVMA, before granting registration in Australia, to re-assess all the data assessed by overseas regulators, to charge fees and to delay commercialisation of products?  I have proposed that:

a.      APVMA only assess those data that relate to aspects unique to Australia, e.g. environmental considerations.

b.      APVMA accept overseas regulatory decisions for those aspects not unique to Australia.

c.      To protect proprietary rights to data, APVMA require applicants to submit all data.  If the full dataset, as used by overseas regulators cannot be provided, the applicant should not be allowed to rely on an overseas regulator’s decision.

d.      Providing the full dataset also allows APVMA to review relevant aspects of the data and, where necessary, engage in informed discussion with overseas regulators.

e.      If a product is registered overseas for similar uses to those proposed in Australia, allow expedited registration with the registrant being required to submit additional required information, including efficacy data, in accordance with a timeline agreed between APVMA and the registrant.

There are additional changes related to operations that I will discuss in the next blog. In the interim, what do you think:

1.      Do we need an improved regulatory system for agricultural and veterinary chemicals in Australia?

2.      How does the current regulatory system affect you decisions with regard to introducing new products into Australia?  Why?

3.      Do you agree or disagree with our proposals for use of overseas regulatory decisions?