An Act to amend the Food and Drugs Act and to make consequential amendments to other Acts

This bill was last introduced in the 39th Parliament, 2nd Session, which ended in September 2008.

Sponsor

Tony Clement  Conservative

Status

Second reading (House), as of June 10, 2008
(This bill did not become law.)

Summary

This is from the published bill. The Library of Parliament often publishes better independent summaries.

This enactment amends the Food and Drugs Act to modernize the regulatory system for foods and therapeutic products, to strengthen the oversight of the benefits and risks of therapeutic products throughout their life cycle, to support effective compliance and enforcement actions and to enable a greater transparency and openness of the regulatory system.
It also amends other Acts in consequence and includes transitional provisions and coordinating amendments.

Elsewhere

All sorts of information on this bill is available at LEGISinfo, an excellent resource from the Library of Parliament. You can also read the full text of the bill.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:30 p.m.
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Conservative

Gary Goodyear Conservative Cambridge, ON

Mr. Speaker, I guess I want to congratulate the hon. member, but I would like to ask him a question. The reason I guess I would like to do that is I was very confused by his speech.

On one hand, he complained that the government did not go out and speak to people, which we did. That is where the amendments and suggested amendments have come from, because we listened to Canadians and stakeholders. He is wrong, even on some of the things he has said himself.

Why would the member come to the House of Commons with a speech like that and mislead Canadians? I spoke with the member yesterday. We talked about all the amendments. He now pretends they did not exist and the bill is a bad bill, yet he knows full well that we are at second reading. This is what we do in the House of Commons. This is where we have debate with members participating. This is where we come up with ideas to make the bills better.

I do not understand the logic that it is somehow wrong to amend a bill. We have proposed certain amendments that will alleviate all the concerns the member has raised in his speech. The member knew that before presenting his speech. I am curious why the member would stand in the House and mislead Canadians in such a fashion.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:30 p.m.
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Liberal

Sukh Dhaliwal Liberal Newton—North Delta, BC

Mr. Speaker, the question of the member for Cambridge is exactly where I wanted to go. I asked the member for a copy of the letter so I could see the amendments. In response he told me that he did not have the letter from the minister to the health committee.

How do we know whether those amendments even exist? We have to assume it. This is exactly the problem with the government. It is very tight-lipped. If it were so open and so honest, then it should share those amendments right here.

The right thing to do is to withdraw the bill and then bring forward the amendments. We should bring the real bill into the House so members can have a real debate on it. It is not only us. My constituents should be able to look at the amendments and make comments on them.

The exact policy of the government is that it does not want to share the information with the grassroots.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:35 p.m.
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Liberal

Larry Bagnell Liberal Yukon, YT

Mr. Speaker, I have three short questions and comments.

First, for the experts on the bill who are watching, as I said in my previous speech, it is very important for one of my constituents that Empowerplus continues to be legally available. I hope they would confirm to me by email or some other means that it is the case.

Second, the member for Cambridge, with whom I mostly agree on this bill, has to understand that the reason the members have asked to consider the bill before second reading is there are so many amendments both by the government and others. The experience we have had in the past is when we get to second reading, we cannot change things that much.

We had an example in one committee where something was changed in a clause from year to two years and the Conservative chair of the committee ruled it out of order, it was too much change. Therefore, we can understand people's hesitancy and why they would prefer the bill to go to committee before second reading.

A question I have for the member is from one of my constituents, Drew. It is very short, but it reflects a concern about which other constituents have also written. He says:

I would not be writing this letter if this bill had no “teeth”, but unfortunately (under section 23) it gives government agents unprecedented power to search, confiscate and prosecute people....

Does the member have any comments on the regulatory and enforcement mechanisms in the bill?

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:35 p.m.
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Liberal

Sukh Dhaliwal Liberal Newton—North Delta, BC

Mr. Speaker, I would like to thank the member for Yukon for his work on this bill, for his speech in the House yesterday, and for his commitment to his constituents.

When it comes to enforcement, many of my constituents are fearful that inspectors will be able to go into their bedrooms and kitchens to find these drugs. They will be put in jail and face a big fine.

We are looking for a third category where we can have legislation instead of regulation, so it is clearly defined by Parliament. Inspectors need to have clear direction from Parliament. This is a concern of constituents in Yukon and also a concern of my constituents in Newton--North Delta.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:35 p.m.
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Liberal

Robert Thibault Liberal West Nova, NS

Mr. Speaker, it has always been my understanding, as a member of Parliament, that when one votes in favour of a bill at second reading, one is voting on the principles of that bill. We expect that the bill will be sent to committee where committee members can work on the details, and work on minor adjustments to the bill to make those principles work. If the amendments are substantive, then the principles are being changed.

In this case the minister has stated both inside and outside the House and at committee that natural health products were not at play in the bill. He said that nothing in this legislation would change the rules for natural health products: the availability, the choice. But I understand from members opposite that the minister now wants to put forward some amendments that would deal specifically with natural health products where they are not involved in the bill now. That is changing the principles of the bill.

I believe that it would be respectful of the House if the minister withdrew the bill, made the relevant amendments, and put the bill forward, so that all members could do an adequate study, receive advice from the Library of Parliament, receive advice from interest groups and professionals prior to our debate at second reading, and well in advance of it going to committee where we would make those moderate modifications.

Does the member not find this to be contemptuous of Parliament? Does he not find it to be disrespectful that members would abuse their privileges in this way?

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:40 p.m.
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Liberal

Sukh Dhaliwal Liberal Newton—North Delta, BC

Mr. Speaker, I have had many discussions with the member for West Nova. He was very kind every time I spoke to him about my constituents' concerns. We had a very open discussion.

The question that he raises is exactly what I meant in my speech. The member for Cambridge had explicit information that we did not have and our constituents did not have. Those amendments would change the intent of the bill.

The member for West Nova said the same thing. It would be better for the minister to withdraw the bill, put the amendments into the bill, and let the bill come back to the House, so that Canadians and parliamentarians could have a real look at it. Parliamentarians could then have an open and transparent debate on the bill to bring out the truth--

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:40 p.m.
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Conservative

Gary Goodyear Conservative Cambridge, ON

You would not understand it, if I wrote it for you.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:40 p.m.
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Liberal

Sukh Dhaliwal Liberal Newton—North Delta, BC

Mr. Speaker, the member for Cambridge can grumble about whatever he wants. He has admitted that he has explicit information that other members do not have. What is wrong with us?

I would suggest that the government should withdraw the bill and note rush it through this Parliament.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:40 p.m.
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Conservative

The Acting Speaker Conservative Royal Galipeau

Order, please. The debate on Bill C-51 has now lasted for more than five hours. Accordingly, the speeches that will follow will be limited to 10 minutes.

I will give the floor first to the hon. member for Verchères—Les Patriotes for a 10-minute speech.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:40 p.m.
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Bloc

Luc Malo Bloc Verchères—Les Patriotes, QC

Mr. Speaker, I am pleased to rise as a member of the Standing Committee on Health, and also as a consumer, to speak to Bill C-51.

The Bloc Québécois has been saying for a long time that there is a lack of surveillance over foods from countries other than Canada. We ask that importers of such products meet standards similar to the ones we have here for products manufactured in Quebec and Canada. The Bloc Québécois also wonders whether these importers should not also be subject to a number of criteria to ensure that public health is not threatened by products manufactured elsewhere.

Of course, Bill C-51 would introduce innovations such as a tracing system, a register of adverse effects especially for drugs, a recall management system, a new measure to eliminate damaging effects on public health. However, the bill also contains slightly vaguer measures that, according to the bill, would be clarified by regulations.

It is because of this vagueness that we must meet in committee with the Minister of Health, in order to find out why the bill leaves so much room for regulations. It is also important that the committee hear experts from various associations and even members of the public. Once the committee has done its work on Bill C-51, we expect the minister to be extremely open to amendments that will improve the bill.

At this point, I would like to mention a few vague provisions that will require clarification when the bill is studied in greater detail in committee. We know that Bill C-51 makes changes regarding drug advertising. Subclause 15.1(2) of the bill prohibits advertising of prescription therapeutic products. I quote:

No person shall advertise a prescription therapeutic product to a person other than a practitioner unless they are authorized by the regulations to do so.

Here, once again, the bill mentions regulations yet to come.

Nonetheless, this regulation would allow prescription drugs to be advertised. It is possible to do so under paragraph 30(1)(h).

The Governor in Council may make regulations for carrying the purposes and provisions of this Act into effect, including regulations... respecting: (i) the labelling, packaging or advertising—or the offering or exposing for sale—of foods, therapeutic products or cosmetics.

Current legislation at least bans the advertising of prescription drugs. However, as we know, it is possible to get around the legislation. There are two choices for advertising drugs: the product can be named but not described and the ad can show people enjoying themselves living a better life, or the problem can be described but not the treatment and people can be told to consult their physician.

We know that the bill appears to be going in precisely the same direction. Consumer associations in Quebec and Canada have asked the government a number of times to plug this loophole.

Perhaps this should be cleared up in committee.

There is also the marketing and approval of drugs. Currently Health Canada is assessing the possibility of setting up a new type of drug licensing called progressive licensing. Bill C-51 includes some of the concepts involved in this progressive licensing approach. It would allow information to be collected and analyzed on an ongoing basis after the drug is marketed. It is only after the drug is marketed that a greater number of people will be exposed to it and that other important data on the drug could be established.

It is good to look at the entire life cycle of a drug to see whether it works. Quite often when clinical trials are done, the number of guinea pigs, as they could be called, is relatively limited, which sometimes prevents us from seeing in detail the possible interaction a drug may have with other drugs the patient is already taking. What is more, as Professor Carleton from British Columbia told us in committee, genetics can also come into play when assessing drugs.

However, considering this approach, we need to ask questions. Will the process be rushed? Will drugs end up on the market before they have been carefully examined? Another question we should ask is whether drugs will be put on the market before they are fully ready to be put on store shelves and in pharmacies.

Subclause 18.7(1) of the bill seems to open the door to that possibility. It states:

Subject to the regulations, the Minister may, on application, issue a market authorization to a person in respect of a therapeutic product other than a designated therapeutic product if the Minister is of the opinion that the person has established that the benefits that are associated with the therapeutic product outweigh the risks.

(2) The market authorization is deemed to be subject to the terms and conditions that are prescribed from time to time.

(3) The Minister may issue the market authorization subject to the additional terms and conditions that he or she considers appropriate.

We would like to speak to the minister to find out, for example, what are the criteria he will use to evaluate and make that decision in accordance with proposed subclause 18.7.

The bill also states that the minister will establish a register where information on adverse effects will be available. Subclause 20.8 of the bill says:

The Minister is to establish and maintain a publicly accessible register in which is to be kept the prescribed information about therapeutic products.

However, we also read in the bill that the information in the register will come only from health care institutions. No register will be set up to gather complaints from consumers or patient associations, for example. Only health care institutions will be able to contribute. What is the reason for this? It would be interesting to hear the minister's response to this as well.

This register raises another question. We currently have the MedEffect register. What will happen to it? Does this mean that this register is ineffective? Once again, it would be interesting to come back to these questions in committee.

The bill also talks about inspectors. This is important. Currently, there are many inspectors who work within the Quebec Ministry of Agriculture, Fisheries and Agri-Food performing the same duties as this bill proposes. These people play an important role in food inspection. We wonder how Bill C-51 would affect these people and if the federal government would be interfering in Quebec's jurisdiction with this bill.

There is also the question of natural health, which—

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:50 p.m.
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Conservative

The Acting Speaker Conservative Royal Galipeau

It is with regret that I must interrupt the hon. member.

We shall now proceed to questions and comments. The hon. member for West Nova.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:50 p.m.
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Liberal

Robert Thibault Liberal West Nova, NS

Mr. Speaker, I would like to congratulate the hon. member on his remarks. He is a diligent member of the health committee, and I cannot help but notice his impressive new haircut. I understand he shaved his head to raise funds in support of people with cancer. What a commendable thing to do.

I am sure he has followed this bill's progress, as have I. All the witnesses who appeared before the committee, not specifically for this bill, but to examine some of the drugs on the market and the drug approval process, generally spoke in favour of progressive licensing for drugs, which this bill specifies.

The member realizes, as I do, that many Canadians were afraid that this bill would make it more difficult to access natural health products. The minister indicated that this bill was in no way meant to target those products or change access to them in any way. It is not meant to make access any easier or any more difficult. It is not meant to change the licences to sell such products or any such matters. He said that was a completely separate issue.

Now we are told the minister intends to make a number of changes to the bill, changes that will affect these products. I think this will change the principles of this bill and I would like to ask the hon. member if he agrees with me.

We were asked to support the principles of this bill at second reading and to study it thoroughly in committee. Now, those principles are being changed. When we go back to committee, it will be with a bill that is different from the one we have been studying so far, the one we have been discussing with experts, the one on which the research branch of the Library of Parliament has been advising us. I would like to hear the hon. member's comments on this.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:50 p.m.
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Bloc

Luc Malo Bloc Verchères—Les Patriotes, QC

Mr. Speaker, first of all I would like to thank my colleague from West Nova who noted my new haircut and also that it was not a moment of madness that led me to shave off all my locks, but a heartfelt gesture in support of children suffering from cancer. Together with 7,300 other participants who shaved their heads, we managed to raise $3,800,000, which will give hope to these children.

With regard to his question on natural health products, at present, there is a great deal of confusion. People are wondering whether the new regulations will contradict the Natural Health Products Regulations. It will be very important for the minister to be clear about this when the bill is studied in more detail in committee. We must allow Canadians to address the committee and we must work together to shed light on the matter and to ensure that all legislation is respected and that people are safely able to use the products they currently turn to.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:55 p.m.
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NDP

Bill Siksay NDP Burnaby—Douglas, BC

Mr. Speaker, I appreciate the comments made by the member and also congratulate him on his support for children with cancer.

He went through many of the problems with the bill and mentioned many of the reasons why I, personally, do not support the legislation and why the NDP caucus is not supporting it either.

I want to raise particularly the question about natural health products and Chinese traditional medicine, which is very important to people in my riding. It is a long and distinguished tradition, maybe even longer than western medicine, yet it seems to be compromised by this legislation.

I wonder if the hon. member could comment as well on that issue and the fact that even the Conservatives now seem to realize that there are very serious flaws with this legislation, necessitating amendments at this particular stage in the process.

Food and Drugs ActGovernment Orders

June 10th, 2008 / 1:55 p.m.
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Conservative

The Acting Speaker Conservative Royal Galipeau

I must inform the hon. member for Verchères—Les Patriotes that he has 30 seconds to comment.