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FederalDid not become law (session ended)40th Parliament, 2nd Session

Bill S-232 explained in plain English

An Act to amend the Patent Act (drugs for international humanitarian purposes) and to make a consequential amendment to another Act

Federal Parliament bill summary, status, timeline, sponsor, votes, and official sources.

At a glance

Jurisdiction
Federal Parliament
Legislature / Parliament
Parliament of Canada
Session
40th Parliament, 2nd Session
Bill number
Bill S-232
Full title
An Act to amend the Patent Act (drugs for international humanitarian purposes) and to make a consequential amendment to another Act
Current status
Did not become law (session ended)
Latest event
At consideration in committee in the Senate
Last updated
Jun 16, 2009

Official Parliament of Canada snapshot for 40th Parliament, 2nd Session. MP vote breakdowns appear when the House of Commons publishes a recorded division export for that bill. Senate and House stage details include official debate/sitting links when LEGISinfo publishes them.

Chamber
Parliament of Canada
Current Stage
At consideration in committee in the Senate
Latest Activity
Jun 16, 2009
Plain-language explanation
In plain English (our explanation)

Our plain-language take, written for civic education.

Source: By PoliticalData.ca

AI-assisted, reviewed before publishing
Short Version

Bill S-232 amends the Patent Act and Food and Drugs Act to allow Canadian manufacturers to produce and export patented drugs to developing countries facing public health emergencies without the patent holder's permission, provided certain conditions are met.

What It Means

Bill S-232 amends the Patent Act and the Food and Drugs Act to make it easier for Canadian manufacturers to produce and export certain pharmaceutical drugs to developing and least-developed countries facing serious public health crises, especially those caused by HIV/AIDS, tuberculosis, malaria, and other epidemics. Currently, manufacturing patented drugs without a patent holder's permission is illegal in Canada. This bill creates a system where authorized Canadian manufacturers can legally make patented drugs specifically for export to eligible countries, without the patent holder's consent. Manufacturers must obtain authorization from the Patent Commissioner and pay prescribed royalties to patent holders. The eligible countries are those recognized by the United Nations as least-developed or listed by the Organization for Economic Co-operation and Development (OECD) as eligible for official development assistance. The bill creates a Schedule that lists all eligible countries. Before exporting, manufacturers must disclose product information on a website, including the drug name, destination country, and distinguishing features. They must also comply with export licensing requirements. Products sold under this program cannot be re-exported to other countries without permission, and some restrictions apply to ensure products are not used for commercial purposes in certain countries. The bill also amends the Food and Drugs Act to exempt drugs made under this authorization from some normal domestic manufacturing requirements, though they must still meet safety standards acceptable to the importing country's regulatory authority or the World Health Organization. The law includes a requirement for the Minister to review the program two years after it comes into force and report results to Parliament.

Uncertainties Or Limits
  • This draft was normalized from a partial local-model response and must be reviewed before publication.
Laws Or Regulations Affected
Patent Act
amended

Substantially modified to create a new authorization system allowing Canadian manufacturers to produce and export patented drugs to eligible developing countries without patent holder consent, subject to royalty payments and export restrictions. Sections 21.01 to 21.2 are replaced or amended to implement this system.

Source: Sections 21.01-21.2

Food and Drugs Act
amended

Modified to exempt drugs manufactured under the Patent Act authorization system from normal domestic drug approval requirements (Part 1), but establishes alternative approval pathways that must be satisfied before export, ensuring products meet acceptable safety standards.

Source: Section 37(2) and new section 38

Generated using AI from official bill text. Not legal advice. It is written by PoliticalData.ca for civic education, automatically checked and spot-reviewed before publishing.

Official text

Parliamentary Process

Step 1
First reading
Mar 31, 2009
Completed

Bill S-232, an act to amend the Patent Act for international humanitarian drug purposes, completed its first reading in the Senate on March 31, 2009.

Introduction and first reading, Mar 31, 2009
End of stage activity, Mar 31, 2009
Chamber sittings
Introduction and first reading - Mar 31, 2009

During a Senate sitting on March 31, 2009, Bill S-232, an Act to amend the Patent Act (drugs for international humanitarian purposes), was introduced and read for the first time, along with several other procedural matters and debates.

Step 2
Second reading
Jun 16, 2009
Completed

The Senate completed its second reading stage for Bill S-232 on June 16, 2009, and referred the bill to a committee.

Second reading, Jun 16, 2009
Referral to committee, Jun 16, 2009
End of stage activity, Jun 16, 2009
Chamber sittings
Debate at second reading - Apr 23, 2009

During a Senate sitting on April 23, 2009, senators heard statements on various topics, presented committee reports, engaged in Question Period on diverse issues, and debated several bills, including Bill S-232 concerning international humanitarian drug access, which was adjourned for further debate.

During the Senate's second reading debate on Bill S-232, the sponsor explained the bill's aim to improve access to medicines for developing countries, after which the debate was adjourned.

Debate at second reading - May 14, 2009

During a Senate sitting on May 14, 2009, debate occurred on Bill S-232, concerning access to medicines for humanitarian purposes, with a senator advocating for its passage due to the current law's ineffectiveness.

Debate at second reading - Jun 16, 2009

During a Senate sitting on June 16, 2009, various procedural matters were addressed, including the debate at second reading of Bill S-232, which was subsequently referred to committee.

This Senate debate on June 16, 2009, included discussions on multiple bills and procedural matters, highlighted by a question of privilege regarding a government website and extensive debate on several legislative items.

Step 3
Consideration in committee
Nov 19, 2009
Not completed

Bill S-232 was being considered by a Senate committee between October and November 2009, but this stage was not yet completed.

Step 4
Report stage
Not reached yet
Not reached

We don't have a plain-language summary for Report stage yet. The official source linked below is the full record.

Step 5
Third reading
Not reached yet
Not reached

We don't have a plain-language summary for Third reading yet. The official source linked below is the full record.

Step 1
First reading
Not reached yet
Not reached

We don't have a plain-language summary for First reading yet. The official source linked below is the full record.

Step 2
Second reading
Not reached yet
Not reached

We don't have a plain-language summary for Second reading yet. The official source linked below is the full record.

Step 3
Consideration in committee
Not reached yet
Not reached

We don't have a plain-language summary for Consideration in committee yet. The official source linked below is the full record.

Step 4
Report stage
Not reached yet
Not reached

We don't have a plain-language summary for Report stage yet. The official source linked below is the full record.

Step 5
Third reading
Not reached yet
Not reached

We don't have a plain-language summary for Third reading yet. The official source linked below is the full record.

Debate and sitting links point to official parliamentary sources when LEGISinfo publishes them. Any plain-language discussion summaries should be generated from those official texts and reviewed before public display.

Vote Summary

No published recorded division

This bill is still active. We only show vote counts after the legislature publishes a recorded division.

Sponsor
Yoine Goldstein
Senator | Details not listed in current Senate roster
Jurisdiction
Federal Parliament

No published representative vote breakdown

This bill is still moving through the process. When a recorded division is published, representative positions can be listed here.

Official sources

Status, sponsor, votes, and timeline on this page are drawn from these official legislative sources and public records. Each summary above is attributed to its own source.

How this data is sourced