opportunities and limitations of bio-pesticide regulatory framework in sub-saharan africa for...
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Presented by Cargele Masso, IITA, at the Regional Experts Workshop on Development, Regulation and Use of Bio-pesticides in East Africa, Nairobi, Kenya, 22–23 May 2014TRANSCRIPT
Opportunities and limitations of bio-pesticide regulatory framework in sub-Saharan Africa for
improved quality, storage and profitability
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Regional Experts Workshop on Development, Regulation and Use of Bio-pesticides in East Africa, Nairobi, Kenya, 22–23 May 2014
Cargele Masso (IITA)
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A substance containing living microorganisms that improve the growth of treated plants by reducing the negative impacts of biotic stress
Bio-pesticide definition in COMPRO-II
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Example of a bio-pesticide
Label claims
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Bio-pesticide regulations: consideration
•Proper labeling to prevent product misrepresentation or
misleading information
•Efficacy for the intended purpose
•Safety to plant, animal, human, and environment when
used as directed
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Findings of a recent study (09-11)
•>90% of products evaluated did meet the quality
standards
•Label claims were not supported by testing results
•Inadequate labeling
•Limited capacity for marketplace monitoring
Labeling of microbiological products
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Mandatory requirements Optional requirements
Product name Brand name
Guarantee analysis Warranty
Directions for use Lot number
Registration number Label claims
Expiry date Complete list of ingredients
Company’s contact info Website
Net weight Storage precautions
Cautionary statement
Planting window (when applicable)
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Partners in participating countries
•Regulatory bodies•Policy makers•Research scientists•Manufacturers of microbiological products•Agricultural professionals•Farmer organizations•Agricultural NGOs•…..
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Participating countries
•Ethiopia•Ghana•Kenya•Nigeria•Tanzania•Uganda
Concluding remarks
Engaging interested stakeholders Official SOPs for quality control Well-defined safety, efficacy, and labeling
requirements Strengthening laboratory capacity (material/human
resources) Capacity development (institutions/good practices)
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Concluding remarks (cont’d)
Awareness creation (end-users) Product registration Marketplace monitoring Well-defined timeframe for file review (registration
processes; SDS)
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