Regulatory scoping
Definition of the product, uses, regulatory status, active-substance sources and working schedule.
- Applicable route
- Document inventory
- Data and study plan
Morocco and North Africa · regulatory affairs
We support manufacturers, importers and distributors in preparing, reviewing and following active-substance and formulated-product registration dossiers in Morocco and North Africa.

Definition of the product, uses, regulatory status, active-substance sources and working schedule.
Coherent organization of administrative, formulated-product, active-substance, analytical, toxicology, residue, environmental, ecotoxicology and efficacy sections.
Cross-sectional assessment to identify gaps, inconsistencies and points requiring technical justification.
Preparation of authority exchanges, additional-information responses and controlled document updates.
Working method
Each stage produces a clear output and a documented decision point.
Before any submission, we check the applicable texts, the authority’s procedure and the evidence required for your project.
Related expertise
The review examines administrative documents, active-substance and formulated-product data, scientific studies, efficacy evidence and labelling. It checks completeness and consistency across the available documentation.
Explore ONSSA dossier preparationA dossier gap analysis compares the available evidence with the requirements applicable to the project. It identifies missing studies, inconsistencies and priorities for completing the dossier.
Explore dossier gap analysisShare the product category, intended uses, target country, number of products and a list of available technical documents. This allows the team to identify the scope of the review and the information still needed.
Request a dossier assessment