Thank you, Madam Chair and members of the committee, for allowing me the opportunity to speak on behalf of the consumer health products industry on Bill C-6. My name is David Skinner, and I'm president of Consumer Health Products Canada, formerly known as NDMAC.
Consumer Health Products Canada is the national industry association representing manufacturers, marketers, and distributors of consumer health products. The association’s members, who range from small businesses to large corporations, account for the vast majority of sales in Canada’s $4.7-billion market for these products. Our members’ sales are equally proportioned between natural health products and other consumer health products, including sunscreens, allergy medicines, upset stomach remedies, and so forth. Our association has been the leading advocate for consumer health products for over 110 years.
Bill C-6, the Canada consumer product safety act, is, along with expected amendments to the Food and Drugs Act, a key legislative component of the government’s food and consumer safety action plan. Consumer health products are exempt from Bill C-6 by virtue of falling under the current Food and Drugs Act definition of “drug”. Nevertheless, we have identified two issues with respect to Bill C-6 that relate to consumer health products within the broader consumer safety action plan.
The first of these issues is the need to ensure that the intent to exempt those products regulated under the Food and Drugs Act is indeed carried out effectively. The second relates to the release of confidential business information to third parties, a provision found in both Bill C-6 and in the former Bill C-51 the Food and Drugs Act amendments that were introduced in the last Parliament and that died on the order paper when the 39th Parliament was dissolved.
The stated intention of the government is to exempt all therapeutic products, including consumer health products, from the provisions of this particular bill. This is to be accomplished by referencing the current definition of “drug” in the Food and Drugs Act. However, there has been much confusion around the need to specify a number of consumer health products to ensure they are adequately excluded through Schedule 1 to Bill C-6. The minister has indicated that an amendment to clarify the scope of the act will be proposed.
A concern has been expressed that if specific subcategories of products broadly defined in Section 2 of the Food and Drugs Act are not set out specifically, they may be subject to the provisions of Bill C-6 in addition to the Food and Drugs Act. It stands to reason, however, that if one subcategory of natural health product is to be specifically identified as exempt, then all subcategories of products captured by Section 2 of the Food and Drugs Act must be set out in Schedule 1 to Bill C-6. Classes of product that must be recognized in addition to NHPs would include personal care products—for example, antiperspirants—and other consumer health products such as sunscreens.
A further concern that we have identified is that while Schedule 1 identifies substances that would be exempt from the provisions of the bill, it is unclear whether this exemption would extend to other elements of the products regulated under the Food and Drugs Act, specifically their packaging and labelling. Discussions with departmental officials thus far have not been able to rule out the possibility that any subcategory of product could wind up being subject to both pieces of legislation in this way. In addition to the complexities and the unwarranted burden of being subject to two pieces of legislation, this possibly also creates the potential for situations in which the two regimes could come into conflict with each other.
Regulations and guidance documents under the Food and Drugs Act set out many specific requirements for the packaging of consumer health products, including child-resistant packaging, tamper-evident packaging, packaging material specifications, dose delivery mechanisms—for example, metered inhalers—and, of course, labelling.
We recognize that an attempt to list all possible classes of product could fail to cover all potentially relevant products. Since new classes of products arise from time to time under the Food and Drugs Act—for example, nutraceuticals—the list could be out of date rather quickly. To ensure that Bill C-6 clearly exempts products regulated under the Food and Drugs Act and to provide for flexibility so that every time a new class is added under the Food and Drugs Act there is no need for consequential amendments to Bill C-6, we recommend that schedule 1 be amended to delete articles 2 to 5 and replace them with a broad exemption for all products regulated within the scope of the Food and Drugs Act.
Our second key concern relates to the confidential business information provisions. The consumer health products industry understands the need, in rare emergency circumstances, for Health Canada to be able to release confidential business information to foreign regulatory authorities and other third parties to mitigate against potential serious and imminent public health risks. However, given the extent of vital proprietary information shared with Health Canada, industry believes that Health Canada must also notify the proprietor of the confidential information at the time such information is disclosed. Since consent to disclose is not required in the circumstances laid out in the act, timely notification would not in any way impact the government's ability to act or to act in a timely manner.
Thank you for your time and consideration of our industry's perspective on this important legislative proposal. My colleague and I look forward to answering questions you may have.