ENVR 401 December 1, 2003 Supervisor: George McCourt Ashleigh Akalehiywot Andrea Hicks Mara Dacso...
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Transcript of ENVR 401 December 1, 2003 Supervisor: George McCourt Ashleigh Akalehiywot Andrea Hicks Mara Dacso...
![Page 1: ENVR 401 December 1, 2003 Supervisor: George McCourt Ashleigh Akalehiywot Andrea Hicks Mara Dacso Ted Walker Lillian Harris Kate Washington Regulation.](https://reader036.fdocuments.net/reader036/viewer/2022062314/56649ef65503460f94c0a2d4/html5/thumbnails/1.jpg)
ENVR 401December 1, 2003
Supervisor: George McCourtAshleigh Akalehiywot Andrea HicksMara Dacso Ted WalkerLillian Harris Kate Washington
Regulation of Biopharmaceuticals in Canada
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Presentation Outline
Client Context of Research Research Question Methodology
RSC Recommendations Government Response Analysis Comparative Studies
Conclusion Suggestions to Client
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Polaris Institute - Ottawa
Biojustice Project, Lucy Sharratt Canadian regulatory system Plants with Novel Traits - Biopharmaceuticals Environmental risks of biopharming
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Context of Research
Regulatory Bodies Canadian Food Inspection Agency Environment Canada Health Canada
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Context of Research
Dir94-08 and Dir2000-07 biotechnology directives
Royal Society of Canada report Action Plan and Progress Reports Interim Amendments to Dir2000-07
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Research Question
Do the most recent Federal Government regulations on Plants with Novel Traits
take into consideration the Royal Society of Canada Report’s
recommendations concerning environmental risks of field testing?
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InterimAmendments
Directive2000-07
Action Plan&
Progress ReportsRSC
(2001)
Government Legislation
Non-government Risk assessment
Government Mandate
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Methodology
Selected recommendations for analysis Assessed government's response: Action
Plan and Progress Reports Analyzed Interim Amendments Identified gaps in Canadian regulation Comparative studies: United States and
European Union
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InterimAmendments
Directive2000-07
Action Plan&
Progress ReportsRSC
(2001)
Government Mandate
Government Legislation
Non-government Risk assessment
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Recommendation 6.3 (Effects of Selection)
potential effects of selection: on an introduced organism or on genes transferred to natural recipients
Concerns: Perpetuation of transgenes within wild populations
RSC Recommendations
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RSC Recommendations
Recommendation 6.6 (Reproductive Biology)
environmental assessments should pay particular attention to reproductive biology obtained from specific experiments
Concerns: Gene flow
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RSC Recommendation
Recommendation 6.7 (Greater Ecosystem Knowledge)
environmental assessments should include potential impacts on natural and disturbed ecosystems
Concerns: Biodiversity; genetic diversity within populations
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InterimAmendments
Directive2000-07
Action Plan&
Progress ReportsRSC
(2001)
Government Mandate
Non-government Risk assessment
Government Legislation
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Action Plan and Progress Report
Focus of Action Plan:•Transparency
•Inspection and monitoring
•Harmonization of CFIA and EC regulation
Although the Action Plan makes reference to specific RSC recommendations, the proposed actions and their implementation deal with the environmental concerns on a general level.
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Action Plan and Progress ReportRec 6.3 (effects of selection)
Effects of Selection now required under New Substances Program of the CEPA
Rec 6.6 (reproductive biology)Not addressed
Rec 6.7 (greater ecosystem knowledge)Canadian Biotechnology Strategy Fund: supports relevant research projects
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InterimAmendments
Directive2000-07
Action Plan&
Progress ReportsRSC
(2001)
Government Mandate
Non-government Risk assessment
Government Legislation
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Interim AmendmentsBiopharmaceutical field testing
Environmental safety measures: Increased isolation distances and
mandatory buffer zone Strict disposal requirements Increased monitoring Contingency Plan
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InterimAmendments
Directive2000-07
Action Plan&
Progress ReportsRSC
(2001)
Gaps
Gaps
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Identified Gaps
Regulation for approval of biopharmaceuticals does not include
• Measures preventing risk to wild ecosystems
• Insufficient precaution• Incentives/funds for further scientific
research
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The Reasons
These gaps exist because one of the following reasons:
a) Concerns not mentioned in regulation OR b) Concerns mentioned but regulation not
adequate OR
c) Concerns addressed through suggestions not requirements
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Research Question
Do the most recent Federal Government regulations on Plants with Novel Traits
take into consideration the Royal Society of Canada Report’s
recommendations concerning environmental risks of field testing?
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Answering the Research Question
The newest Canadian regulation (interim amendments) does address some additional environmental concerns as recommended by the RSC report, but key elements still missing
• Further research to gain empirical knowledge• Greater precaution until more knowledge
acquired • More comprehensive regulation to prevent
danger to ecosystems
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Employs "Best Science" Framework
Regulatory Bodies U.S. Department of Agriculture - Animal and
Plant Health Inspection Service
Environmental Protection Agency Food and Drug Administration
Comparative Study ~ United States
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Biopharming in the United States
Exclusivity of farm equipment Isolation distance vs closed-pollination Temporal isolation
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Based on "Precautionary Principle"
Moratorium No field testing of biopharmaceuticals
Comparative Study European Union
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Conclusions
RSC raises specific environmental concerns
Interim amendments partially reflect RSC concerns
U.S. imposes additional precautions in field testing
E.U. restricts testing of biopharmaceuticals
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Suggestions to Client
Empirical knowledge Effects on non-agricultural ecosystem Restrictions on confined field testing Explicit rather than suggestive
language
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Everybody is welcome to join us for a GMO-free beer at
Hurley’s Irish Pub.
First round’s on George!