Thank you, Mr. Chair and members of the committee.
My name is Keith Mussar. I am with I.E.Canada, the Canadian Association of Importers and Exporters. It is a privilege to appear before the committee to testify with respect to Bill S-11, the safe foods for Canadians act.
I.E.Canada, the Canadian Association of Importers and Exporters, is a national trade association that has been speaking on behalf of the Canadian trade community for more than 80 years. Our members include food manufacturers who import and export food, Canadian importers and exporters, wholesalers, distributors, and Canadian grocery retailers. We represent some of the largest food manufacturers, importers, and exporters in Canada, as well as small and medium size businesses. Our members import and export food across most food categories.
Bill S-11 will replace and modify the existing statutes governing food safety, packaging and labelling, and inspection under the Meat Inspection Act, the Fish Inspection Act, the Agricultural Products Act, and the food-labelling provisions of the Consumer Packaging and Labelling Act. It will also introduce new requirements on businesses that manufacture, import, and export food.
The bill provides authority to the minister to issue a licence to persons authorizing them to import, export, or convey food from one province to another. This builds on the CFIA regulatory initiative that will license importers of food in the non-federally registered sector. The bill extends the authority of the minister to license all food importers and exporters. In addition, the bill provides the minister with the authority to prescribe conditions to license, such as the requirement to implement a preventive food safety control system as a condition for obtaining and maintaining a licence.
The bill would allow for a number of other improvements, including tougher penalties for non-compliance, enhanced powers of the inspectorate, and consistent inspection and enforcement across all commodities. Also, the bill could provide for the creation of regulations to establish pre-clearance requirements for any imported food commodity. The latter could facilitate the movement of imported food commodities into Canada and would be consistent with provisions being proposed under the U.S. Food Safety Modernization Act .
While the objective to increase food safety is clear, the bill as currently written will have severe negative implications for Canadian food manufacturers and Canadian consumers. First, Canadian food manufacturing jobs will be lost. Canadian jobs will be moved to the United States or other foreign countries. Second, Canadian food exporters will lose access to foreign markets. Third, Canadians, particularly those in ethnic communities, will have less choice of safe, healthy, and nutritious foods. The following examples serve to illustrate these concerns.
First, many Canadian food manufacturers produce food exclusively for export to and sale in the United States or other foreign countries. It is common for such products to contain ingredients that are not permitted for use in Canada, yet are allowed in the foreign country of destination. Such products cannot be sold in Canada as they are not compliant with Canadian regulations. Clause 12 of the bill, which prohibits a person to have in his possession for the purpose of exporting a prescribed food commodity, unless it meets the requirements of the Canadian regulations, will preclude the manufacture of such products in Canada. Multinational companies that have manufacturing plants both in Canada and the United States will have no choice but to move the manufacture of these products from Canada to the United States.
Second, subclause 10(3) of the bill prohibits a person from exporting a prescribed food commodity unless the food commodity meets the requirements of the Canadian regulations. In other words, a prescribed food commodity that is exported to a foreign country must meet the requirements of the Canadian regulations as well as those of the foreign country of destination. This requirement will limit the export of Canadian manufactured products to foreign countries. For instance, the food and drug regulations require Canadian milled flour to be fortified with vitamins such as folic acid. Canadian manufactured products such as cookies, crackers, pasta, and breaded fish products, to name a few, if required to contain fortified flour, will not be allowed access to countries in the European Union, where fortification of flour with folic acid is prohibited.
Canadian companies are allowed under current Canadian regulations to import product that does not comply with Canadian regulations, provided it is brought into compliance before being offered for sale in Canada. This is allowed without prior notification to CFIA. CFIA inspectors visit Canadian companies and ensure compliance of these products with Canadian regulations as they would for any domestic manufacturing facility. This practice is used in particular to correct non-compliance related to food product labelling and often on products for smaller market segments, such as ethnic markets. Correction of non-compliance prior to sale is a cost-effective and efficient alternative to producing products in unique packaging exclusively for the small Canadian market. The prohibition to import non-compliant product under subclause 6(2) of the bill will prohibit this practice and limit food choices, particularly for consumers in small market segments.
In addition, it is estimated that 50% of the volume of spices imported into Canada are further processed in Canada to be made safe for consumption and compliant with Canadian regulations. The prohibition to import products that are not compliant with section 4 of the Food and Drugs Act will preclude the importation of such raw spices into Canada, resulting in the loss of these Canadian processing jobs.
I.E.Canada members have also raised concern regarding two other aspects of the bill.
First, the unrestricted authority for inspectors to take photographs under paragraph 24(2)(g) raises concerns over security and the possibility of intentional or unintentional disclosure of confidential information, such as processing, equipment design, and function. Many companies have taken steps to prohibit the use or possession of cameras, cellphones, and other devices with picture-taking capability by employees and guests in manufacturing facilities to minimize this risk.
Second, incorporation of documents into regulations by reference is an important authority that will allow regulations to maintain currency and allow for changes in a timely manner that will keep pace with the rapid changes in innovation. While desirable, a process is required to ensure stakeholder consultation is undertaken to allow those impacted by a change to have an opportunity to express their views. Additionally, a process is required to ensure that proposed changes to documents incorporated into regulation by reference are communicated internationally and an opportunity is provided to those impacted to provide comment.