Structured support for registration in Morocco
MCARE helps companies prepare, review and follow their dossiers while considering administrative, scientific and local requirements.
- Gap analysis and regulatory strategy
- Identification of missing data and documents
- Preparation and review of technical summaries
- Coordination of studies and partners
- Preparation of responses to authority questions
From initial review to procedure follow-up
Each stage is documented with responsibilities, deliverables and a timeline.
1. Gap analysis
Dossier review and prioritisation of gaps.
2. Document plan
Studies, letters, certificates, summaries and additional information.
3. Compilation
Organisation, drafting, consistency checks and submission preparation.
4. Follow-up
Support for clarifications and coordination of technical supplements.
Cross-sectional scientific and administrative review
Administrative & identity
Applicant, manufacturer, sources, certificates, composition and labelling.
Scientific data
Physico-chemistry, toxicology, residues, environment and ecotoxicology.
Biological efficacy
Uses, rates, GEP trials, selectivity, justification and agronomic consistency.
Identify risks before submission
An early review helps reduce inconsistencies, missing data and delays.