NAVIGATING YOUR COMPLIANCE
Trusted Regulatory Expertise for Plant Protection Products (PPPs)
Our team assists manufacturers and distributors in registering active substances and formulated products throughout North Africa and the Middle East.
3+Countries covered
6+Years of expertise
100+Registration files handled
Understanding Registration
A legal authorization based on scientific evidence
Registration confirms that the product is effective and that its risks are acceptable under the proposed conditions of use.
The assessment examines human and animal health, residues, environmental fate, non-target organisms, efficacy, selectivity and regulatory compliance.
Registration Tools
Every tool from the presentation, organized as a clickable section
The eight sections are available from this homepage, the main menu and the complete Registration Tools page.
01
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
About Us
Deep expertise in plant protection product regulatory affairs
We transform complex regulatory frameworks into clear, actionable pathways from strategy to final decision.
- Multi-country knowledge across North Africa and the Middle East.
- Technical expertise across every scientific dossier section.
- End-to-end support through authority assessment.
Our Services
Regulatory support across the whole product lifecycle
Registration Dossier Compilation
We build and format dossiers in line with national guidance, including REF/HP/05/14 in Morocco. The formulated-product package covers identity, physicochemical and technical properties, toxicology, analytical methods, application data, efficacy, selectivity, classification and labelling. The active-substance package covers identity, properties, analytical methods, toxicology, metabolism, residues, environmental fate, ecotoxicology and classification.
Product Lifecycle & Portfolio Extension
We manage renewals, regulatory surveillance, use and portfolio extensions, multi-brand strategies, dose and PHI changes, revised conditions of use, ownership transfers and supplier updates.
Authority Liaison and Compliance Management
We perform completeness checks, organize submission, prepare responses to additional-information requests, update documentation and manage administrative follow-up through final validation and publication.
PPP Efficacy Trials & Scientific Studies
We coordinate with accredited GEP/GLP organizations for sample importation, field application, data collection, statistical analysis and extrapolation. We cover efficacy and selectivity trials, residue studies for MRL and PHI validation, and physicochemical, toxicological and ecotoxicological studies involving bees, birds, aquatic organisms and other non-target species.
Our Process
How we guide your registration
Initial Consultation and Regulatory Scoping
Assess company status, product nature, data-protection profile, target uses and countries.
Regulatory Classification
Determine the correct category, applicable chapter and evidence pathway in each target country.
Dossier Preparation
Collect, structure and validate identity, physicochemistry, analytical methods, toxicology, residues, environmental fate, ecotoxicology and efficacy data.
Submission and Follow-up
Submit to the competent authority and manage additional information, amendments and follow-up through the final decision.
Where We Operate
Registration procedures across the Maghreb
Morocco
ONSSA · Law 34-18 and applicable technical references.
Algeria
MADR · Executive Decree No. 95-405 and commission submission route.
Tunisia
DGPCQPA · Decree 2010-72 and national dossier requirements.
