Evaluate product performance
Compare your product with a suitable control or benchmark. Depending on the scope, measure crop growth, yield, quality, nutrient uptake, root response, and visible crop injury under defined greenhouse conditions.
Bringing a fertilizer or supplement to Canada? AGS helps manufacturers, importers, and distributors plan greenhouse trials, evaluate crop response, and organize technical evidence for discussions with CFIA or your regulatory adviser.
Discuss Your Fertilizer ProjectCompare your product with a suitable control or benchmark. Depending on the scope, measure crop growth, yield, quality, nutrient uptake, root response, and visible crop injury under defined greenhouse conditions.
Bring together product information, intended use, existing studies, trial protocols, and results. Identify unanswered technical questions and where specialist laboratory analysis or regulatory advice may be needed.
Develop the technical trial plan alongside the applicable research and import requirements. Confirm responsibilities for site arrangements, product handling, containment, and disposal before work starts.
Some fertilizers and most supplements require CFIA registration before importation or sale in Canada. Requirements depend on the product, ingredients, intended use, and applicable exemptions. CFIA’s pre-market assessment focuses on safety information and labelling; a successful crop-performance trial does not replace those requirements.
AGS provides trial design, independent evaluation, analysis, and technical reporting within an agreed scope. CFIA determines regulatory requirements and makes registration and authorization decisions. AGS does not issue CFIA approvals or guarantee an application outcome.
Objectives, treatments, comparison, replication, application rates, measurement schedule, and analysis plan.
Methods, data summaries, statistical analysis, findings, and limitations, including inconclusive or unfavourable results.
An organized account of available product information, study findings, and outstanding questions for your regulatory discussions.
Where the agreed scope includes application-related technical support, AGS can prepare trial descriptions and summarize relevant findings for your submission team. Specialist safety testing and regulatory representation are scoped separately where needed.
How AGS approaches independent third-party validation →Do not assume a performance trial is a registration requirement. CFIA’s fertilizer assessments focus on safety and labelling. AGS can evaluate agronomic performance while you confirm the product-specific information needed for registration with CFIA or your regulatory adviser.
Research provisions may apply, but eligibility, authorization, and import requirements must be checked for the specific product and trial. Contact AGS before shipping so the technical scope and required confirmations can be planned together.
Yes. We can review the design, data quality, analysis, and interpretation. The report identifies the source of the data and distinguishes an independent review from a trial that AGS conducted or monitored.
Share the product category, intended crop and use, country of manufacture, current registration status if known, available studies, and your timeline. Begin with a high-level description; confidential formulation details can be discussed through an agreed transfer method.
Discuss Your Fertilizer ProjectAn enquiry does not commit you to paid work. Scope, deliverables, timing, and fees are agreed before paid work begins.
Product-specific requirements should be checked against current CFIA guidance.