Mr. Speaker, I am pleased to rise today on behalf of the constituents of Newton—North Delta and the official opposition of Canada to participate in the debate on Bill C-28, an act to amend the Food and Drugs Act.
This enactment would amend the Food and Drugs Act to provide the Minister of Health with the authority to issue interim marketing authorization for foods that contain substances at specified levels, and to exempt those foods from the applicable requirement of the act and its regulation relating to their sale.
The proposed amendments are in response to concerns raised by the Standing Joint Committee for the Scrutiny of Regulations regarding an administrative process put in place by Health Canada under the regulations of the Food and Drugs Act to allow Canadians faster access to food products under specific circumstances. All members of the House want our food supply to be safe, efficient and effective.
The bill proposes to amend the Food and Drugs Act to achieve two purposes. First, to provide the Minister of Health with the authority to issue an interim marketing authorization for the early sale of safe food and safe food products that contain certain substances; and second, exempt any food that contains an agricultural chemical, at or below the maximum residue limit specified by the minister under the new Pest Control Products Act, from the prohibition in the Food and Drugs Act of the sale of foods containing these residues because the sale of these foods would not pose harm to consumers. We are talking about safety.
The bill would give the minister authority to issue interim marketing authorization for food products wishing to enter the market earlier or that have previously entered the market and have added or modified contents since initially approved by Health Canada.
Currently, the deputy minister of health responsible for health products has the authority to issue interim marketing authorization, IMA. The minister is arguing that the authority to issue the IMA is a power of Parliament granted by the Crown and therefore the responsibility for the IMA should rest with the minister.
The bill would also allow for food products which contain pesticides, veterinary pharmaceuticals or added vitamins, minerals or amino acids at or below the maximum residue limit to be exempt from the FDA regulations while in the approval process.
Briefing material provided by Health Canada argues that Canadian companies are currently at a great disadvantage because of the lengthy approval time for new or modified food products. Canadian companies are not on a level playing field with their trading partners, particularly in the American market. This is because the U.S. government allows food products in the approval stage to be marketed, given that they are not harmful and not restricted by any other law or legislation.
The amendment that we are debating would put Canada on a par with the United States and give our food producers a level playing field when it comes to new products entering the market.
We would not be here today were it not for the Standing Joint Committee for the Scrutiny of Regulations. Bill C-28 is a direct consequence of concerns first raised by that committee in April 1999. At that time, over five years ago, the committee identified the regulations of the Food and Drugs Act permitting interim marketing authorization as illegal. In other words, it was not supported by legislation.
Much of the law that affects Canadians is not found in the statutes of Canada, but in the thousands of regulations made pursuant to powers granted by acts of Parliament. Each year the federal government introduces about 1,200 new regulations. Since 1975 the federal government introduced over 28,000 regulations. That is 122,000 pages of regulations. About 20% of the laws in the country stem from legislation debated and passed in this legislature. The remaining 80% of the laws that we see are made up of regulations; just 20% is what we passionately debate in the House.
After a debate, we vote yea or nay, depending on the merit of the proposed law. The media and the general public focus on the 20% component. However, the 80%, which is coming through the back door by way of regulations, is not debated nor are other parliamentary democracy principles applied to those regulations.
Regulations on the other hand, receive virtually no debate in the House or even the other place, no public policy input, no studies or media scrutiny. This is an affront to democracy. Under parliamentary reform, this is the one the main issues at which we must look.
My private member's Bill C-205 passed in the House. I thank all members for their support. What will the bill do? We all know the government rules, but does not govern through the complete parliamentary democracy and practice. Some 80% of the regulations, which comprise the law, are made under the authority of Parliament. Various agencies, bodies or quasi-government organizations are delegated the authority to make regulations. However, when they make regulations, Parliament does not have the authority to scrutinize or review those regulations.
Therefore, a big chunk of our laws have been completely ignored. There is a big black hole in accountability and democracy which has been ignored for so long until Bill C-205 passed. With the passing of the bill, Parliament now has the authority to review regulations of those agencies through the Standing Joint Committee for Scrutiny of Regulations. They will now be scrutinized and if need be, disallowed.
My bill restored some of that democracy. It was a huge step in parliamentary reform. We talk a lot about reform, but little action is taken.
The Standing Joint Committee for Scrutiny of Regulations does the only scrutiny. Very limited scrutiny of regulations is done in Parliament. Our new regulations are permanently referred to the committee pursuant to the provisions of section 26 of the Statutory Instruments Act. Members of Parliament and Senators are on the committee. Legal counsel and staff work diligently, scouring through thousands of papers on dry, technical, legal subject matter as part of their thankless task of reviewing regulations.
This committee is generally misunderstood and ignored. This committee is considered to be not a very high profile committee, despite the hard work it does. In fact, talking about parliamentary democracy, this committee should be considered a very important one. It is an essential watchdog, protecting democracy, controlling bureaucracy and holding the government to account.
The standing joint committee does not judge regulations on the basis of policy measures, general merit, or necessity. Its study of regulations is instead limited to the questions of validity and legality. Members follow uniform and clearly defined criteria in their examinations. Compared to most committees, this committee is non-partisan and we build consensus in the committee.
The committee judges whether or not an statutory instrument: is not authorized by the enbabling legislation or is not in compliance with the conditions set forth in the legislation; does not conform with the Canadian Charter of Rights and Freedoms or the Canadian Bill of Rights; purports to have retroactive effect without express authority being provided by the enabling legislation; imposes a charge on public revenues, imposes a fine or imprisonment without express authority; excludes the jurisdiction of courts; has not complied with the Statutory Instruments Act with respect to transmission, registration or publication; appears to infringe on the rule of law, trespasses unduly on rights and liberties, make rights and liberties unduly dependent on legislative discretion, makes some unusual or unexpected use of powers conferred by the enabling legislation; amounts to the exercise of power that should properly be the subject of parliamentary enactment; and is defective in its drafting, including the translation.
These criteria deal with matters of legality and procedural aspects of regulation, not the merits of the regulations or policy.
The committee works meticulously, and with the complex nature of its undertaking, work proceeds at a slow pace. The long delays in dealing with particular items are largely related to the large number of regulations which the committee has to review relative to the number of meetings it can hold each year. All this considered, the committee, with the able assistance of its long-time legal counsel, Mr. Francois Bernier, is remarkably productive. Consider that over the period from November 7, 1997 to December 6, 2001, the committee dealt with 1,133 pieces of subordinate legislation in the course of 45 meetings.
I am a seven term co-chair of the Standing Joint Committee on Scrutiny of Regulations, representing all members of the House and I speak from personal experience. The work of the committee members can be extremely frustrating. We in effect hold ministers accountable for the legality of subordinate legislation, primarily regulations, sponsored by their departments.
However, this task is at times almost impossible. When the scrutiny of regulations committee finds a regulation that it deems in conflict with the legislation, our first step is to inform the respective department in writing. It should be a simple process. We identify a problem regulation, inform the department and then it fixes it. Instead, what we usually encounter is foot-dragging that can carry on for years or even decades.
The Food and Drugs Act regulations are an example of this foot-dragging. For five years, the department argued that there was nothing wrong with the regulations concerning the notice for interim marketing authorization. We are debating this today. Finally, after so many years, the department abruptly informed the committee last April that it was proceeding with the legislation before the House today. For over five years, the department has been using illegal regulations. Those are the regulations we are trying to correct today.
In a democracy that prides itself in the rule of law, this is unpardonable, but it is not the least bit unusual. Recently, my committee finally closed another file that had been opened for 27 years, more than a quarter of a century.
The committee's usual practice is to deal with a problem regulations informally by letter to the relevant officials. This allows the minister involved to amend the regulation with minimum fuss. The committee can also prepare and issue a disallowance report, but this is usually done only after the department has failed to address our previously identified concerns. Disallowance reports are very rare.
Let us consider the sequence of events surrounding the Food and Drugs Act regulations concerning interim marketing authorizations. I want to give this example so that the members in the House, the public in general, and our media scrutiny can also understand and comprehend the problems facing this committee.
On April 7, 1999 counsel for the scrutiny of regulations committee wrote to the DIO and questioned the legality of provisions of food and drug regulations that provided for notices of interim marketing authorization. The objection was that these provisions provided for unauthorized exemptions and also involved an illegal sub-delegation of powers.
On November 25, 1999, 232 days later, the department responded that it considered the provisions to be a valid exercise of regulation-making powers conferred by the Food and Drugs Act.
On December 23, 1999, the committee counsel reviewed the arguments put forward by the department and sent a letter countering those arguments, asking for reconsideration.
On March 8, 2000, now 355 days, almost a year after the initial correspondence and over three months since the last letter, the department replied indicating that generally it was committed to the policy, but that it might review the regulatory provisions in question with a view to making a “clarifying amendment.”
Exactly seven months later, on September 28, 2000, the committee was forced to again write to the department to inform it that it wished a detailed response to its letter of December 23, 1999.
Nothing more was heard from the department until October 17, 2001, over one year since the last correspondence, when a comprehensive reply to the letter of December 23, 1999 was finally received by the committee.
On December 12, 2002, the file was re-submitted to the joint committee with a 13 page note on the October 17, 2001 response.
On March 3, 2003, myself, as co-chair of the standing joint committee, wrote to the Minister of Health to restate the committee's position and explain why the response from the department was not accepted.
Over a year later, on June 24, 2004, the committee was informed that:
It is the intention of the Department to bring forward legislation in the early Fall 2004 that will amend the Food and Drugs Act to allow the Minister of Health to issue NIMAs and provide for a limited power to exempt food products from the application of the Food and Drug Regulations and paragraph 4(d) of the Act.
Finally, on November 29 Bill C-28 was introduced. There was a little over five years between the time the issue was first raised with the department and the introduction of remedial legislation. As I said earlier, when compared to other files that stretch on for decades, this issue was resolved rather quickly. However, five years is still five years. That is far too long for illegal regulations to remain in place.
Departments and their ministers take far too long to respond to concerns of the committee. There is no good reason for the department to go over a year without responding to a letter from the committee. It is an affront to the rule of law, it is an affront to Parliament and it is an affront to democracy. That is why we need Parliament to be reformed, including scrutiny of regulations issues.
I support Bill C-28. The amendments to the Food and Drugs Act are years overdue. I give full credit to the members, the staff and the counsel of the Standing Joint Committee for the Scrutiny of Regulations for identifying the drawbacks in the system, bringing that to the fore, and following and chasing it through until remedial action is taken by the department to correct this parliamentary affront that has been going on so long.
I will conclude by asking members of Parliament to look into the regulatory process so that the regulatory process in this country is fair, efficient and effective.