:
Thank you very much, Mr. Chair.
[Translation]
Good afternoon, honourable members of Parliament and distinguished participants.
Thank you for inviting us to appear today to provide you with an update on the activities of the Health Canada Pest Management Regulatory Agency since we last met in February 2007.
[English]
We have submitted to you today a report that outlines key activities of our agency, showing recent trends, and it provides updates on key issues involving the agriculture sector. Trends are presented for a number of activities, including new active ingredient registrations, minor use registrations, and review performance. Some notable agency successes are presented, including the approval of the first NAFTA-labelled pesticides, Canada's participation in global joint reviews with its Organization for Economic Cooperation and Development counterparts, and the introduction of a new policy for the registration of generic pesticides.
[Translation]
I, or my colleague Richard Aucoin, the Chief Registrar, would be pleased to answer questions on this material. I will take a few minutes to highlight some of the activities that have provided, and will continue to provide, benefits for Canadian growers while maintaining strong protection standards of human health and the environment.
[English]
One of our accomplishments over the past few months is the ongoing implementation of an improved system for registering generic pesticides. We consulted on and made improvements to our data protection policy as requested by grower groups and industry.
The primary goal of our new policy is to provide fair protection of the proprietary interests in data to encourage the introduction of new and reduced risk pest control products, while at the same time providing a predictable timely process for the introduction of competing generic pesticide products to the Canadian market.
I'm also proud to report that we've seen a substantial increase in the number of reduced-risk chemicals and bio-pesticides, which is indicative that registrants are seeing the benefits of registering new technologies in Canada, and that they're not deterred by regulatory requirements.
This increase has, however, slightly affected our ability to meet our review performance target of 90% for category-A submissions in the first two quarters of the 2007-08 fiscal year. Where we didn't meet performance standards, our delays were typically limited to under two months. However, in the same timeframe, we've registered more new active ingredients in major new uses in this fiscal year—that's the first half of this fiscal year—than all of last fiscal year.
New resources from the recent “Enhancing Access to Pest Management Tools” Treasury Board submission are expected to help resolve this drop in review performance, as well as contribute to our ongoing initiatives related to agricultural competitiveness. For example, we continue to work on key initiatives aimed at increasing the availability of newer, lower-risk pesticides for growers in Canada.
The minor use program, a collaboration between Agriculture and Agri-Food Canada and Health Canada, as well as active-ingredient-targeted projects, such as Project 914, have yielded hundreds of new minor use registrations in the last year. Project 914 was piloted for three new active ingredients selected based on input from grower groups such as the Canadian Horticultural Council. To meet a six-month review timeline, we made use of the United States Environmental Protection Agency's data package and reviews for these same active ingredients. In 2007 these registrations yielded 479 new minor uses for growers from a wide range of agricultural sectors.
[Translation]
The agency is also involved at the international level on this issue, participating in the first Global Minor Use Summit in the fall of 2007. On the topic of international collaboration, we continued to work to address the areas where streamlined processes would benefit Canadian growers.
[English]
This is evidenced by recent successes such as the registration of three NAFTA labels, Canada's participation in the first ever global joint review of a new active ingredient, and the fact that over 40% of new active ingredients registered in Canada go through joint reviews or work-sharing with the United states or global partners such as Australia and Europe.
NAFTA labels allow the free movement of product across the U.S.-Canada border to the benefit of growers on both sides. Many other products have been nominated as NAFTA label candidates, including new products undergoing joint review. These activities provide Canadian growers access to new products at the same time as their competitors with a built-in price discipline mechanism, which was the preferred solution recommended and strongly supported by every grower association represented on the own use import task force in 2006.
This brings me to my next topic, the grower-requested own use import program, GROU. Since our last meeting in February 2007, and in keeping with the recommendation of this committee, we maintain growers' access to the OUI product ClearOut 41 Plus while implementing the new GROU. In a recent development, the manufacturers of ClearOut 41 Plus announced their intention to make available to growers the Canadian-registered version of their product, which has been registered since early 2006. Although they intend to distribute the product through one supplier only, the result is that growers will no longer have to apply for an OUI import permit in order to access this popular generic herbicide.
As for the OUI task force members' commitments, grower groups in the pesticide industry continue to collaborate on the growing list of available of GROU products. This program allows growers in Canada to import the U.S. version of a Canadian-registered product if it is available to their competitors at a lower price.
There are currently six approved GROU products, with an additional seven submitted for review. These products represent a wide range of uses and meet the needs of growers from across Canada in all commodity sectors.
The GROU nomination committee, made up of all key national grower groups as well as the Canadian Federation of Agriculture, is the body responsible for making submissions to the PMRA for consideration in the GROU program. This group has a number of additional priority products that are under discussion for possible submission to the program.
Finally, we continue to work on re-evaluating older pesticides using modern scientific standards. In some cases registrants are required to add new mitigation measures to their labels in order to satisfy today's environmental and health risk assessments. One example affecting the agriculture sector is the addition of buffer zones to older pesticides in order to protect environmentally sensitive areas and allow the continued registration of that pesticide in Canada.
These buffer zones can pose challenges to growers, and we have committed to work with grower groups and the provinces on buffer zone issues as we try to balance the goals of environmental protection and agricultural sustainability. For example, in March we'll be holding a workshop with stakeholders, including grower groups, to discuss buffer zone issues.
[Translation]
I would like to stress that our primary mandate is the protection of human health and the environment. The initiatives that we have undertaken are intended to provide our growers with the necessary tools to remain competitive in this increasingly competitive global market, while continuing to ensure that human health and the environment are protected.
[English]
We hope to continue the positive momentum that has been achieved over the past few years with the agricultural sector.
Thank you, and I look forward to answering your questions.
:
Good morning, Madam Dodds. I thank you and Mr. Aucoin for appearing.
We have had many meetings with PMRA over the past number of years that I've been involved in this committee. If there is one agency that has probably been named as being a bit of a thorn in farmers' sides, it's the way PMRA has worked in the past. But I believe we have moved beyond that to a point where I see some progress, and this is possible today probably thanks to a lot of your work. I like to be complimentary whenever I can, and I think this is one time we ought to recognize the work done.
As Canadians we've always talked about the kind of work we need to do towards harmonization, towards getting products that are used in the United States also being allowed to be used here.
The argument that is always made is that if you can buy a tomato that's grown in California and it is grown under a different product label, which is not allowed here, yet we allow the tomato to come in, why wouldn't that be allowed here? We keep getting those arguments. We talk about labelling and that we need a better identity of Canadian product, and what does “Canadian product” mean.
We didn't come here to talk about labelling, but I think it all goes back to the argument that can be made by a consumer and certainly can be made by farmers as to why are we not more flexible or perhaps more in tune in terms of the harmonization of products.
I didn't have an opportunity to look at the report here, which just came, so I'm sure some of that material is there. But perhaps you could bring us up to speed and tell us where we were four years ago compared to where we are now. And I know what you're trying to do is to give us some progress reporting. Could you just bring us up to speed as to where we were, where we are now, and how much more quickly the system is working today than it did four years ago?
:
One of the chief advancements is the current practice of doing joint reviews with the United States. It's really in our favour to do that. With new actives, when they're undergoing joint review, the experience is that they're then introduced to both the U.S. users, the farmers, and the Canadian users, including farmers, at the same time with the same maximum residue limit applied for the pesticide.
And more and more, as I said in my opening comments and as you'll see in the report, we're undertaking these joint reviews. So that is helping to make sure that U.S. and Canadian farmers have access to the same pesticides at the same time.
Through projects such as 914, we've also worked to address some of the older products--not necessarily very old, just within the last number of years--where the United States registered products and they weren't brought to Canada, and we have then looked at those products, using U.S. reviews, and it's really expedited the timeline. So, as I mentioned, within six months we reviewed and registered these actives under Project 9l4, which resulted in hundreds of minor uses, which is very favourable.
Is there anything you wanted to add, Richard?
Thanks for being here this morning.
We're doing a review, and we're trying to improve the system to make it easier for our producers to have a level field with those they compete with in the world. We've heard over and over again, “Why can't we use these products? They can use them there, and yet we're importing their food.” You know, that whole story. We know that sometimes we don't have a level playing field, because we have various organizations such as the WTO and NAFTA, which often make it difficult for us to institute a buy-Canadian policy in our institutions. We've seen that response from the government to our recommendation to the reports. In other words, we have all these trade challenges that we have to be careful of when we're doing business.
There is a growing number of Canadians who are worried about what they call the security and prosperity partnership, which in a nutshell is advocating more or less a complete harmonization of all aspects of our economies, not only agriculture, but other aspects of our life. A number of people are concerned. They see that often this means, or can mean, a lowering of standards, and of course there are health concerns.
The question is, if in part this can be the case when we're looking at various products for our farmers and for Canadians, how we get a balance where we keep in mind that we have to look at health concerns, but at the same time ensure that we can assist our producers to get that level playing field.
The fruit growers in my area have mentioned to me that there are actually better products that are more environmentally sound that Americans are using, that are better for the environment and for health, that we can't get here, and we have to use the old ones that are more damaging. So this is the other way where harmonizing would be better.
So I guess my question is, do we have a certain standard that we say this is it, when we're doing this--we're not going to get below this? Does this fit in not only with what's happening in North America, but does it address some of the standards that are in Europe, for example, in the European Union, which often, in regard to pesticide residue levels, are higher than what we have? How do you come up with an answer that meets the needs of our producers, that meets the needs of the health of Canadians? I'm just wondering if you could maybe shed some light on this. These are questions I'm thinking of and people are asking me.
:
I'll try. It's a difficult subject.
To protect human health, countries around the world have an absolute standard below which they will not go. We do as well. Protecting human health, we say, and the environment, are our primary mandates. But the act is clear: we have to consider the competitiveness of the agriculture sector and we have to consider providing tools--pesticides--to users in Canada.
For human health, when you think of consuming residues on foods, there is, based on the toxicity of a pesticide, an absolute amount that we won't let you consume above. Now typically, in any country, a number of pesticides are contributing to that amount. The difficulty comes because we don't have the same multiples of pesticides registered in every country.
In Canada, if I say, for chemical A, that we have ten products that have chemical A in them and we're going to make sure you don't consume above this amount, we might set an MRL of ten for each of the ten. In the United States they might have 200 different pesticides that have that active in it. They might have to set a lower MRL to make sure that the total consumption doesn't go above that level. They might have two pesticides and could set a higher MRL to make sure you don't go above that consumption.
The reaction of the human body to a chemical remains the same no matter if you're here, in California, in Cuba, in New Zealand, or in Japan.
With respect to the effects on the environment, that can be quite different. It obviously depends very much on the kind of environment in which you're using a pesticide. For example, we know that sun decomposes or breaks down most pesticides. So if you're in a tropical country with a lot of sunlight, the level of pesticide in the environment is likely to deteriorate faster with time than if you're in Canada, which has a northern climate. You're trying to control both environmental exposure and human health exposure through the use of the pesticides. Because they can be used on many different foods, you have this concern about maximum residue limits and differences all over.
When we look at safety, we look at the toxicity of the pesticide. We look at, in Canada, what foods it's used on and what foods are imported into Canada with potential pesticide residues. We have data on what Canadians consume, and that goes from infants right through to seniors, broken down by subpopulation group and gender. We synthesize all those things when we're setting an MRL.
There is often the ability to protect human health and protect the environment and change an MRL and change use, but sometimes there isn't.
:
In reality, those cost recovery fees—I've been informed by CFIA about some of their on-farm cost recovery fees—are almost at breakeven. Forgetting about the cost recovery fees and dropping the administration.... The administration cost for some of this cost recovery is fairly extensive as well.
Mr. Chair, we need to consider whether to make a recommendation that the money, at least if it's there, go back to where it would lower the costs to industry in some fashion, rather than go into general revenue. This is money that's one way or another coming directly out of farmers' pockets.
This leads me to my second question. One key area of concern, which we constantly hear about from the farm community, is that our regulatory systems—CFIA, PMRA, cost recovery for other programs, environmental programs, and so on—add a burden to Canadian farmers' costs and put them at quite a substantial disadvantage in the marketplace compared with their competitors.
It was mentioned here earlier by someone that we're not allowed to use a certain product, but that our competitors in Mexico, China, or wherever are. The theory is we're not allowed to use that product because it shouldn't end up on the grocery store shelf; however, our competitors' product ends up on the grocery store shelves.
We have to either get to a system where we're on a level playing field or not allow our competitors' products in. We have to get there, because farmers are getting more and more peeved about this situation.
I think you've recognized that. But has PMRA done any analysis, or do you know of any that's been done, which in a chart form or whatever compares our cost recovery in Canada from producers and other costs in our system that Canadian farmers face, either directly or indirectly, that American farmers, say, don't face—or do?
I'm told consistently that our cost regime is much higher than others' and puts Canadian farmers at a disadvantage. We have to level that playing field, because farmers in Canada have had enough of being disadvantaged by regulatory regimes and seeing competitors' products come in here when they don't have advantage.
I'll give you an example from the hog industry, and not related to you. A hog producer went broke two weeks before Christmas—and there are lots of them going broke. One feed additive that he couldn't get for five years in Canada would have made a difference over that five-year period, in his 800-sow operation, of some $470,000—just that one feed additive. This doesn't relate directly to you; it's another regulatory authority. But that's what it means on the ground, on the farm. We have to level this.
The question is, do you have any analysis, and if you have, can we get it?
:
All of that is the kind of information we'll need to bring forward when we propose—if we propose—changes to our cost recovery regime. There are different costs to different parties, and we have to look at that. I think Mr. Easter raised this too, in terms of the impact on the growers themselves of our cost recovery regime.
Costs for registrants have in some respects gone down, because as I said, they can now submit exactly the same data package to Canada and the United States. We've heard from them that because they can submit it to us electronically, that saves them potentially a couple of hundred of thousands of dollars.
Some of our costs have changed because of things like joint reviews, but they haven't really gone up or down. For example, the pre-submission considerations that go into a joint review are now very complex. You're working with four, five, six different countries and discussing who is going to do what part of the review. For example, Richard and people are travelling, often to Paris, where other countries and registrants are, and they're spending a whole day simply discussing a submission and which country will review what part of the submission.
We haven't had enough experience at the global level yet to really be able to say what the cost of doing that kind of work is versus the cost of doing a distinct Canadian review. We have started doing some of the international comparisons and have had discussions with, for example, the U.S.—I don't know whether we've now had them also with the U.K.—to discuss what their practice is and what their costs are for their parts of the system so that we can also compare the costs in Canada to the costs in the United States and the costs in Europe. I think Australia is also one of the countries we'll be looking to compare costs with.
All of that is the kind of material we'll need to bring forward if and when we talk about changes to the cost recovery regime.
As I said, our experience over the last few years is that some of where the costs come from is shifting, and it's too new in the experience to really realize cost savings, because indeed there is, if anything, more examination because all the different scientists are very interested. But it builds a robustness into the system. Our findings are that when our scientists talk to the U.S. scientists, they come to a common conclusion when they're discussing it as they're reviewing data, versus what we know historically, that you isolate the two sets of scientists and invariably they come to different conclusions.
One of the great benefits has been the development of this MRL calculator. With the United States, we've come to agreement that this is how we will establish a maximum residue limit, so we now know that if you put the same data in, you'll get the same MRL north and south of the border. We did not have that before.
Richard took that to the OECD. Has that been accepted now by the OECD, largely?