Atlantix Agrochemicals guides manufacturers, formulators and importers through every stage of pesticide registration in Kenya and across East Africa — from dossier preparation to final regulator approval.
Atlantix Agrochemicals was founded in Nairobi to solve one recurring problem: agrochemical companies with sound products losing months to registration paperwork they were never set up to manage. We take the file off your desk and run it to completion.
Our team combines regulatory affairs specialists, agronomists and dossier writers who have sat on both sides of the submission process. We know what reviewers look for, which data gaps will stall an application, and how to structure a dossier so it moves through the queue without repeated queries.
Whether you are registering a single formulation or building a portfolio across the region, you get one point of contact, a documented timeline, and a clear view of every outstanding requirement.
The core registration package bundles renewals and compliance, regulator submission, data gap analysis and dossier preparation into a single engagement. Every service below is quoted per trial, after an initial review of your existing data.
Renewals and compliance, regulator submission, data gap analysis and dossier preparation delivered as one end-to-end engagement — from the first audit of your existing studies through to filing, reviewer queries, certificate issue and ongoing renewal management.
Field trial design and supervision with accredited research stations, producing the efficacy data regulators require for crop-specific label claims and dose recommendations.
Residue trial programmes run to GLP standards, with sample analysis through ISO 17025 accredited laboratories and residue data prepared for maximum residue limit submissions.
Harmonised dossiers for Uganda, Tanzania, Rwanda and Zambia, with country-specific label adaptation and local agent coordination where required.
A typical product registration runs through five stages. Here is exactly what Atlantix delivers at each one, and what stays with you.
| Stage | What we do | Included |
|---|---|---|
| Product review | Week 1–2 | Confidential review of your formulation, existing studies and target crops, with a written feasibility opinion and indicative timeline. |
| Data gap analysis | Week 2–4 | Checklist audit against PCPB requirements, a prioritised list of outstanding studies, and costed laboratory quotations from accredited partners. |
| Dossier compilation | Week 4–10 | Full dossier assembly — chemistry, toxicology, ecotoxicology, residues, efficacy and label text — formatted to the regulator's template and internally quality-checked. |
| Submission & liaison | Month 3–9 | Filing with the regulator, tracking of the review, and preparation of responses to every technical query raised during assessment. |
| Post-registration | Ongoing | Certificate handover, renewal calendar, GHS safety data sheets and label maintenance for the life of the registration. |
Timelines assume complete source data at the start of the programme. Where new studies must be commissioned, we build the laboratory lead time into the schedule before submission.
“A registration is not a form. It is a chain of evidence — and every link has to hold.”
From the laboratory bench to the field trial and the regulator's desk — the evidence behind every registration we file.
Regulatory services quoted per trial
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Tell us what you are trying to register. We will review the file, flag the gaps and give you a realistic timeline before you commit to anything.
Send us the product name, active ingredient and target market. We reply within two working days.