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Health Products and Food Branch (HPFB) - Roadmap for 2007-2012

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  1. About the Road Map
  2. Strategic Plan 2007-2012 - Commitments
  3. Blueprint for Renewal II
  4. Strategic Plan 2004-2007- Achievements

1. About the Road Map

The purpose of the Roadmap is to provide an overview of key Health Products and Food Branch (HPFB) strategic frameworks: the 2007-2012 Strategic Plan, the Blueprint for Renewal and the 2004-2007 Strategic Plan.

In the sections below you will find the strategies and commitments laid out in the current plan and a review of the achievements that stemmed from the 2004-2007 Strategic Plan. For further information see the Blueprint for Renewal main page.

2. Strategic Plan 2007-2012 - Commitments

Launched in April 2007, the HPFB 2007-2012 Strategic Plan lays out six main strategies, and lists a number of commitments which will contribute to the implementation of each strategy. These strategies and commitments, as well as the timeline for each commitment, are listed in the table below.

Strategy Commitment Timeline commitment
Strategy 1: Adopt a lifecycle approach to regulating health products 2007-2008
  • Review of the Special Access Program (sap)
  • Review of the Clinical Trials Regulatory Framework
  • Develop and implement new regulatory frameworks for vaccines, radiopharmaceuticals, cells, tissues and organs, and blood
2007-2010
  • Natural Health Products regulatory review
  • Implement a new compliance and enforcement strategy for health products
  • Establish clear and consistent product categorization regime
  • Strengthen regulatory foresight and scientific advice to sponsors
2007-2012
  • Establish and implement Progressive Licensing Framework (PLF) for pharmaceuticals and biologics
  • Implement post-market surveillance strategy
  • Strengthen leadership on issues related to specific populations
Strategy 2: Promote health through a modernized food regulatory system and a proactive approach to nutrition 2007-2008
  • Develop and implement new regulatory frameworks for food related health claims
2007-2010
  • Develop and implement regulatory modernization strategy for food and nutrition
  • Implement the food borne contaminants initiative for the Government's Chemical Management Plan
Strategy 3: Advance international co-operation and be an International leader 2007-2012
  • Engage in international co-operation, harmonization and worksharing
Strategy 4: Establish strategic partnerships to fulfill our mandate 2007-2008
  • Develop and implement Science Plan 2007-2012
Strategy 5: Better integrate transparency, openness and accountability into our day-to-day work 2007-2008
  • Implement policy on Public Input in the review of health products
  • Registration and disclosure of Clinical Trials
Strategy 6: Build a nationally-based, flexible organization that can fulfil its mandate and priorities in a changing environment 2007-2010
  • Establish new electronic review systems for the branch
  • Support Health Canada legislative renewal initiative

3. Blueprint for Renewal II

The revised Blueprint for Renewal II builds on the original policy framework of the first document and offers more comprehensive and detailed plans related to the implementation of the various objectives and initiatives. It focuses on the full range of legislative, regulatory and policy issues needed to modernize our approach to health products and food. For detailed information on the Blueprint, see the Blueprint for Renewal main page.

4. Strategic Plan 2004-2007 - Achievements

Launched in April 2004, the HPFB 2004-2007 Strategic Plan laid out five key strategies, with key results and performance indicators. The achievements stemming from each of these strategies are outlined in the table below.

Strategy Year(s) Achieved Achievement
Strategy 1: Transforming branch efficiency, effectiveness and responsiveness as a regulator 2004-2007
  • Cleared submission backlogs for pharmaceuticals and biologics and medical devices and met performance review targets
  • Implemented Natural Health Products regulations
  • Expanded cooperation with international regulatory authorities
2006-2007
  • Developed cells, tissues an organs regulations
  • Launched and consulted on Blueprint for Renewal
Strategy 2: Providing authoritative information for healthy choices and informed decisions by Canadians 2004-2007
  • Developed new Product Monograph template
2005-2006
  • Implemented nutrition labelling regulations
  • Launched MedEffect website
2006-2007
  • Published the revised Canada 's Food Guide
Strategy 3: Increasing responsiveness to public health issues and vigilance over safety and therapeutic effectiveness 2004-2007
  • Strengthened post-market surveillance and compliance and enforcement
  • Strengthened Clinical Trials oversight
2005-2006
  • Established the Office of Pediatric Initiatives
  • Establishment of two new regional adverse drug reactions monitoring offices
2006-2007
  • Supported Trans-Fats Taskforce
  • Launched Food-Borne Contaminants Initiative
Strategy 4: Improving transparency, openness and accountability to strengthen public trust and stakeholder relationships 2004-2007
  • Published series of reports outlining Branch plans and performance
  • Regularly published Summary Basis of Regulatory Decisions
2005-2006
  • Conducted two groundbreaking public forums on COX-2 and silicone gel-filled breast implants
  • Developed Public Involvement Framework
2006-2007
  • Consulted and implemented policy on public input in the review of health products
Strategy 5: A nationally- based, flexible organization that has the capacity to fulfill its mandate and priorities in a changing environment 2004-2007
  • Developed new technologies to support e-review of product submissions
2005-2006
  • Implemented Branch Audit and Evaluation Office
2006-2007
  • Created and staffed Branch Science Advisor position and Office of Science and Risk