Programme leadership
Investcent is the implementing entity. Detailed responsibilities will be formalised in programme agreements.
An indicative €23.0 million donor funding envelope over 48 months, supporting grant-led research, innovation, demonstration, capacity and scale-up.
No donor approval, EU award or funding commitment is claimed. Allocations are proposed and subject to appraisal, due diligence and agreement. Enquiries do not constitute commitments.
Eight work packages. One integrated programme. The proposed allocation connects delivery capacity with research quality, safeguards and measurable learning.
Amounts are in EUR millions. The allocations total €23.0M. No co-financing or secured contribution is assumed.
Investcent is the implementing entity. Detailed responsibilities will be formalised in programme agreements.
A proposed steering structure, technical review and independent evaluation will support decisions, research ethics and evidence quality. Membership is not yet confirmed.
Proposed controls include documented procurement, segregation of duties, milestone reporting, audit access, conflict-of-interest declarations and complaints pathways.
Governance arrangements, reporting schedules and donor-specific requirements remain subject to agreement.
| Risk | Proposed control |
|---|---|
| Disease outbreaks & biosafety | Approved research protocols, veterinary coordination, sample-handling procedures and outbreak response planning. |
| Farmer adoption & exclusion | Participatory co-design, accessible training, inclusive recruitment and feedback-led delivery. |
| Data privacy & quality | Informed consent, minimised data collection, role-based access, retention rules and record-quality checks. |
| Financial misuse & delivery delays | Due diligence, documented procurement, financial reconciliation, staged delivery and independent audit. |
| Environmental & animal-welfare harm | Environmental screening, waste-management procedures, welfare protocols and responsible antimicrobial practices. |
| Weak institutional uptake | Early institutional engagement, tested operating models, agreed ownership and evidence-led handover. |
The eight work-package envelopes remain the working baseline. Unit costs, quantities, expenditure categories and annual disbursements have not been supplied; no detailed amounts are invented.
Coordination staff time, oversight, procurement and financial reporting; avoid double-counting shared services.
Number and scale of milk-handling demonstrations, research design, equipment specification and cold-chain operating costs.
Surveillance coverage, veterinary time, visits, sample referrals, diagnostics and authorised preventive-service coordination.
Recruitment capacity, cohort size, extension visits, training accessibility and cost per unique farmer.
Identifier choice, hardware, software lifecycle, offline support, interoperability, maintenance and data-quality checks.
Verified laboratory capacity, test panels and volumes, consumables, quality assurance and equipment procurement.
Institutional engagement, operating-model validation, handover resources and replication activities.
Baseline and evaluation sample design, independent verification, research protocols and knowledge products.
Appraise personnel, equipment, research, training, field operations and monitoring within each work package. Identify indirect costs separately if applicable. Contingency and co-financing are not assumed; neither has been evidenced.
Link Year 1–4 costs to annual delivery gates, procurement lead times and activity volumes. Annual amounts remain unallocated until the cost model is validated; €5.75M per year is not an agreed profile.
Use documented specifications, competitive selection proportionate to value, due diligence and conflict declarations. Separate purchasing, approval and payment; retain bid evaluations, asset registers and audit trails. Donor thresholds remain to be agreed.
Propose a steering body for strategic oversight and a technical review function for methods, ethics and quality assurance. Publish membership and terms only after appointment. Evaluators should be independent of implementation decisions.
Screen demonstrations before approval; manage laboratory waste and manure risks; include accessible participation and a confidential complaints pathway. Agree escalation, resolution timelines and safeguarding responsibilities before fieldwork.
Use competent veterinary oversight, humane handling, approved sampling, safe transport and waste disposal. Agree adverse-event reporting and stop-work criteria; vaccination and treatment follow authorised guidance.
Minimise personal data, obtain appropriate consent and establish access controls, retention, correction and incident response. Assess obligations under Kenya’s Data Protection Act and applicable research requirements before collecting field data.
These are proposed principles, not adopted institutional policies. Named oversight members, complaint contacts, procedures and donor-specific requirements must be formalised before implementation.
For institutional donors, foundations, DFIs and research and implementation partners.