Thank you very much.
Mr. Chairman and members of the committee, I'd like to start by thanking you for inviting Consumer Health Products Canada to provide our industry's perspective during the committee's review of a prospective comprehensive economic and trade agreement between Canada and the European Union.
Consumer Health Products Canada is a national industry association representing manufacturers, marketers, and distributors of consumer health products. The association members, which range from small businesses to large corporations, account for the vast majority of over-the-counter natural health products sold in the Canadian market.
The consumer health products industry is a mature but growing segment of Canada's health care system, currently generating approximately $5 billion in sales per year and contributing to the growth of the Canadian economy by providing high-quality employment for over 6,000 well-paid, highly skilled people involved in production, importation, and marketing of consumer health products in Canada. We further estimate that an additional 25,000 retail and distribution positions are supported directly by the sale of consumer health products.
We're aware that the negotiations between Canada and the EU thus far, as well as the discussions of the committee during these deliberations, have touched on various elements of intellectual property for prescription pharmaceuticals, including data protection, patent term restoration, and rights of appeal. We would note that these aspects of intellectual property do not currently exist, nor do they apply in the same manner for consumer health products. Our sector is in dire need of some data protection to ensure that we are attracting research investment to Canada and creating jobs for Canadians in domestic manufacturing and distribution of innovative products.
We believe that government and industry must work together so that Canadians can benefit from new scientific and technological breakthroughs in the area of consumer health products. But with that said, there are currently impediments to innovation in the regulation of consumer health products, which cause multinational corporations to negatively view the Canadian environment and its adverse effect on their ability to gain a return on investment when introducing innovative products.
One of the ways in which our industry innovates is by conducting research on established prescription drugs to find novel uses for them in the consumer market. When safety and patient benefits are demonstrated, this research is then used by Health Canada to process regulations for making a prescription drug available for self-care use.
Canadians benefit in several ways when medicines are switched to non-prescription availability, either for consumer self-selection or through the supervision of a pharmacist. They can treat common ailments and troublesome conditions more effectively without having to make a doctor's appointment. The prescription-OTC switch of antifungals for yeast infections, benzoyl peroxide for acne, and H2 blockers for heartburn are all great examples of this. For industry, switching from a prescription to a consumer market provides the opportunity for innovation.
However, there are also enormous benefits to the Canadian health care system and to the broader economy in switching products appropriate for self-care from prescription to consumer status. Research conducted for our association this year showed that visits to the doctor for colds, headaches, and heartburn cost the health care system $1 billion annually for adults alone. Once children and the associated costs of prescription drugs and lab tests are included, the figure exceeds $2 billion for just three of the hundreds of minor ailments that can be self-treated with consumer health products.
Prescription-to-OTC switching can reduce these costs in multiple ways. In some instances, just making incremental improvements to the self-care options available in the existing categories can generate substantial savings. For example, a Queen's University study showed that switching non-drowsy allergy medications to self-care status produced $65 million in net annual savings on doctor visits, dispensing fees, and drug costs in Ontario alone.
In other instances, by providing an entirely new self-care option, the impact on health care can be more dramatic. For example, in the switch of nicotine replacement therapy for smoking cessation to self-care status, not only were unnecessary doctor visits reduced, but overall quitting attempts rose significantly, contributing to the sharp drop in smoking rates in Canada since the 1997 switch of these products.
For the majority of Consumer Health Products Canada's multinational member companies, innovation happens on a global scale. After investing in the rigorous research to support the safe use of a new product for the consumer population, companies decide within which global markets to file registrations. Jurisdictions that offer data protection or market exclusivity for switched products are the most attractive to industry because they offer the opportunity to recuperate the exorbitant costs of research.
The lack of a data protection period currently being offered to our industry in Canada is causing us to lag many years behind companies in the European Union. As an example of this, in a recent comparative review of the switch landscape in Canada versus the United Kingdom, it was found that between 1984 and 2009, 96% of the switches occurred first in the United Kingdom before Canadians had access to them. Of those products switched first in the United Kingdom, the average period of time before Canadians had access to them was 7.3 years.
A great example of the detrimental effect on the health of Canadians and our economy by the lack of data protection for the consumer health products industry can be seen in the prescription to over-the-counter switch of cholesterol-lowering medications in the European Union. In Canada, competitors are able to get to market within a few short months of the innovator by using the efforts of the innovator to gain regulatory approval.
It is unlikely that any Canadian manufacturer will view this environment as worthwhile to invest in this kind of innovation. Therefore, Canadians will wait many years before accessing a product that citizens of the European Union currently have access to. This switch alone is projected to bring billions of dollars' worth of cost-effective health care savings through reduced coronary heart disease, morbidity, and mortality. With that said, we must also consider the trade opportunity lost for improving the Canadian economy during those lag years by creating thousands of jobs in domestic research and manufacturing and sales.
It's for this reason and many others--outlined for the committee in our written brief--that we propose that Canada align with the European Union's Article 74a data protection period for one year for prescriptions to OTC or prescriptions to natural health product switches when the government relies on proprietary clinical trials of an innovator to approve this change in classification.
Thank you for your time today. Given the complexity of these issues, I would be more than happy to answer any questions you may have.