01
Regulatory strategy
Classification, scope, and pathway.
Specialized service
End-to-End Registration
A complete technical and strategic process to bring a product to market through a consistent and traceable dossier.
How we approach it
A directed pathway, with clear scope and control at every stage.
02
Research and development
Technical basis and validations when applicable.
03
Trials
Efficacy and pre-harvest interval work according to product and use.
04
Critical assessments
Toxicological and environmental components.
05
Dossier and filing
Preparation, submission, and document control.
06
Follow-up
Responses to requirements through the final decision.
What to expect
The scope is activated according to product nature, country, and type of procedure.
Scope, deliverables, and responsibilities are defined for your product, country, and objective. You retain visibility of progress and receive expert judgment at key decision points.
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