Fast-track your pesticide registration with us Today
What we do
PESTICIDE REGISTRATION & CONSULTANCY SERVICES IN KENYA
Conventional pesticide registration
Fast-track the registration of generic or patented conventional pesticides based on chemical active ingredients e.g Mancozeb, imidaclopride, etc.
Bio-pesticides registration
Registration of biological pesticides based on living organisms or plant/animal extract e.g. Bacillus thuringiensis, Trichoderma asperellum, Neem extracts, etc.
Bio-stimulants registration
Registration of Bio-stimulants – natural or synthetic substances that enhance plant growth e.g. Humic & Fulvic Acids, Seaweed Extracts, Amino Acids, etc.
Agency Representation
We offer agency representation for companies across the globe who want to register and sell their agricultural inputs in Kenya. We do all the leg-work with the local authorities for you.
regulatory affairs consultancy
At Talyne AgriScience, you get detailed, professional and up-to-date consultation services at all stages of your product registration services from choice of active ingredients & crop/pest combinations to dossier prep & post-reg support
Business Development Support
Get business development support and insights across your entire product development cycle including market entry strategies, updated market surveys and data, product positioning and marketing strategies, etc.
WHY CHOOSE US?
Key services & Benefits
We offer full-stack registration support from Pre-registration consultation to post-registration support.
Here is what you can expect
- Customized niche Market survey and insights
- Pre-registration consultancy
- Thorough analysis of proposed Chemistries/substances
- Efficacy and performance
- Toxicological profiling
- Product lifecycle forecast
- Data-driven market size & product volume projections
- Preparation of a regulatory strategy.
- Data gap analysis & advice on data requirements.
- Dossier preparation and submission to PCPB/KEPHIS
- Liaison with the Regulatory Authorities.
- Defending the product dossiers at the authorities.
- Initiating, managing and follow up of field efficacy trials with the selected researcher to completion.
- Compilation of product risk assessment reports
- Post-trial follow-up on final product approval at the authorities
Post Registration Product administration and management
- Agency representation
- Label extensions
- Parallel/Daughter registrations
- Label updates
- Product renewals
- Periodical insights on changing regulatory policies.