1. Pre-registration
Optional pre-application meeting and experimental permit for research or field trials.
Registration Tools
Registration Process
From pre-registration through review, every step supports a structured assessment of the application.
The registration process involves many steps, from initial preparation through the final decision. Specific steps may differ by country according to available human, scientific and financial resources.
2. Registration
Dossier submission, administrative and completeness checks, technical and scientific evaluation, risk-management decision, registration number and publication.
3. Post-registration
Record archiving, field monitoring, Rotterdam Convention notification where relevant, label changes, appeals or litigation.
4. Review
Periodic re-registration or unscheduled review leading to renewal, amendment or cancellation.
Other tools
Continue exploring the regulatory framework
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Registration Strategies
Select an approach suited to available resources, evidence and the regulatory framework of the target country.
Open section02Registration Process
From pre-registration through review, every step supports a structured assessment of the application.
Open section03Data Requirements & Testing
Define the studies needed to demonstrate product efficacy and safety through internationally accepted protocols.
Open section04Assessment Methods
Apply procedures and models suited to each scientific component of the dossier.
Open section05Risk Mitigation
Define effective, practical and communicable measures to reduce health and environmental risks.
Open section06Decision Making
Connect risks, values, alternatives and management measures to reach a regulatory decision.
Open section07Registration Criteria
Verify that the product meets general protection goals and applicable scientific and legislative criteria.
Open section08Assessment of Alternatives
Compare available options when a product is highly hazardous or its risks are difficult to manage.
Open section