Fresh Produce Distribution
Safety, traceability, and partner coordination across supply networks.
Inside this journey
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Customer Discovery
Align on desired outcomes, current assortment, quality standards, seasonal constraints, stakeholders, and success metrics for fresh produce supply.
Discovery Questions
Tell Me About Your Produce World
- Walk me through the categories you personally manage and which three take the biggest share of your weekly volume or margin pressure.
- How often do you place replenishment orders for those categories?
- Which of these best describes your current supplier mix for those categories?
- On a typical delivery week, what feels most time-consuming or emotionally draining about managing those categories?
- How confident are you that on delivery day your teams can sell through planned volume without quality-driven markdowns?
Are You Settling for ‘Good Enough’ When Inventory Breaks?
- When a load arrives below expected quality or fill, what immediate decisions do you make and who on your team feels the pressure first?
- How often do out-of-spec shipments cause you to take product out of inventory, mark down, or return?
- Which performance failings hurt you most: inconsistent fill rates, short shelf life, traceability gaps, or delivery timing? Rank your top two.
- Tell me about a recent instance when a supply problem impacted sales or shopper trust—what happened and what kept you up that night?
- How do these recurring issues influence your relationships with category managers, procurement, and store ops?
When the Shelf Looks Wrong, Who Feels It First?
- If a supplier change created fewer surprises, what would change in your week-to-week responsibilities and stress levels?
- Who are the decision-makers and approvers for changing a primary supplier or adding a new distributor for a category?
- How do you quantify risk when a new supplier is proposed—do you weight quality, cost, fill rate, or traceability more heavily? Choose up to two.
- Describe a recent supplier decision that went well—what signals convinced leadership to switch or expand?
- What internal approval timelines and gate reviews would a trial need to pass to become a primary sourcing relationship?
What Would a No-Surprises Week Look Like?
- Imagine one week where every inbound case hit your targets—what specific metrics would make you call that week a success?
- Which numerical thresholds matter most to you for a trial: acceptable fill rate, minimum shelf life on receipt, and quality score? Pick a range for each.
- How should traceability be demonstrated in an ideal scenario—by lot-level visibility, rapid recall response time, or documented chain-of-custody? Choose all that apply.
- What emotional benefit would reliable deliveries bring—less firefighting, better promotions, higher shelf confidence? Which matters most?
- If we achieved your ideal week for two consecutive months, what business changes would you expect (reduced shrink, increased sales, fewer emergency buys)? Be specific.
Where Seasonality Breaks Trust (And How You Solve It)
- Which seasonal transitions create the biggest fill or quality gaps for you (domestic-to-import, region change, harvest change, weather events)?
- How long does it typically take you to notice a supply gap during a seasonal handoff, and what do you do first?
- What contingency strategies have you tried (safety stock, alternate pack sizes, different ripening profiles, dual-sourcing)? Which worked and which backfired?
- How much flexibility do you need from a supplier during transitions—can they change pack size, delivery cadence, or source region quickly?
- Tell me about one seasonal failure that cost you margin or shopper trust—what signs were missed and what would you want different next time?
How Do You Really Qualify a New Supplier?
- When a new distributor asks to run a trial, what are the non-negotiable qualifications they must meet before you consider samples?
- Which certifications and audit standards do you require or prefer? Select all that apply.
- Describe how you score sample shipments—what dimensions (appearance, firmness, shelf life, packaging, labeling) and what scoring scale do you use?
- How long does your internal QA and procurement team need to complete a sample review and decide to move to a trial?
- Would you be open to a co-designed acceptance matrix where we propose targets and you adjust thresholds for a pilot? If so, how hands-on would QA be?
- Who on your side needs to sign off on QA findings and trial progression? Please list roles and, if possible, names.
If We Ran a Trial, What Would Make It a Win?
- If you had to agree to a short trial (4–6 weeks, 2–3 categories), what outcomes would make leadership comfortable expanding the relationship?
- Pick the acceptance criteria you would require to call the trial successful (choose up to three).
- What cadence of checkpoint reviews would you prefer during a trial—weekly scorecards, biweekly operational reviews, or a single end-of-trial audit?
- Which commercial terms matter most during a trial: price guarantees, short-term SLAs, limited-volume commitments, or flexible exit clauses?
- What integrations or operational handoffs must be in place before the first sample—EDI/POS, routing windows, label specifications, or repack instructions?
- Who would own escalation and day-to-day checkpoints on your team during the pilot? Please include role and preferred contact method.
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Solution Experience
Use the buyer’s real categories and failure modes to show how our sourcing, cold-chain, ripening, and QA processes deliver consistent fill rates, shelf life, and traceability.
Experience Meetings
- Current-State Diagnosis — Categories & Failure Modes
- Consequence Quantification Workshop
- Proof-of-Value Walkthrough — Live Flow with Buyer Data
- Operational Readiness & Traceability Validation
- Decision & Next-Steps — Trial Launch Readiness
- A validated recall simulation demonstrates traceability and escalation within the buyer's required timeframe.
- One-sentence Future State (confirm)
- Demonstrate concrete proof that seller processes produce the defined future-state outcomes for each category.
- Obtain explicit buyer validation (or precise objections) on each proof point and its measured impact.
- Agree a set of live sample shipments and QC scoring method to be executed as the next step for empirical validation.
- Seller to prepare and schedule 2–3 instrumented sample shipments with telemetry and QC scoring for the agreed categories (owner: Seller Ops).
- Buyer to provide receiving-window logistics and on-site contact for sample acceptance and QC scoring (owner: Buyer Receiving Lead).
- Both to finalize the QC scoring sheet and acceptance rubric to be used during sample evaluation (owner: Seller QA and Buyer QA).
- Both QA teams to finalize and sign the sample shipment acceptance rubric (owner: Seller QA & Buyer QA).
- Confirm Traceability SLA and Data Access
- Operational owners for traceability, QA, and logistics are named and agree to SLAs and runbooks for sample trials.
- Introductions & Meeting Objective
- Clear pass/fail and remediation rules for sample shipments are documented and accepted by both parties.
- Seller to enable buyer test access to the traceability portal and schedule a 15-minute access verification (owner: Seller IT).
- Ops teams to confirm telemetry device counts, placement, and data delivery method for each sample SKU (owner: Seller Logistics).
- Summary of Findings & Validations
- A mutually signed trial launch plan with agreed success metrics, timeline, owners, and approval gates.
- A scheduled first-sample shipment window and mid-trial review on the calendar.
- Contingency steps identified and accepted for known execution risks.
- Both parties to sign and store the Trial Launch Plan (scope, metrics, timeline) in the shared workspace (owner: Seller AE).
- Seller to schedule and execute the first instrumented sample shipments within the agreed window (owner: Seller Ops).
- Buyer to confirm receiving staff and QA availability for sample acceptance and scoring (owner: Buyer Ops Lead).
- A single, explicit one-sentence current-state for each target category that all participants approve.
- A prioritized list of category-specific failure modes paired with the exact evidence required to quantify them.
- Clear assignment of data owners and deadlines for the evidence needed in the Solution Experience.
- Buyer to share 4 weeks of fill-rate, returns, claims, and POS for each nominated category (owner: Buyer Category Manager).
- Seller to prepare template for failure-mode evidence mapping and upload to shared workspace (owner: Seller Ops Lead).
- Schedule the Consequence Quantification Workshop and circulate pre-read with a data checklist (owner: Seller AE).
- Recap Confirmed Current-State Sentences
- An explicit consequence statement (dollars, time, and risk) for each prioritized failure mode.
- A ranked list of 2–3 categories to use in the Solution Experience based on quantifiable business impact.
- Preliminary measurable acceptance thresholds defined for each selected category.
- Seller to deliver the consequence workbook with populated numbers and sensitivity ranges (owner: Seller Data Analyst).
- Buyer to validate and sign off the prioritized category list and the proposed acceptance thresholds (owner: Buyer Category Manager).
- Both parties to agree on anonymized sample orders to be used in the live walkthrough (owner: Seller AE and Buyer Ops).
- Define Current State (one sentence per category)
- Confirm Trial Scope, Metrics & Timeline
- Diagnosis — Link failure mode to root cause
- QA Protocols & Sampling Plan
- Present Cost Model & Assumptions
- Proof — Walk the actual process with buyer data
- Telemetry & Cold-Chain Exception Handling
- Scenario Walkthroughs
- Roles, Owners & Approval Gates
- Map Failure Modes to Evidence
- Escalation & Recall Simulation
- Tieback — Explicitly map how each proof eliminates the failure cost
- Risk Acceptance & Contingency
- Risk & Compliance Exposure
- Assign Data Owners & Pre-work
- Sign-off & Next Meetings
- Validation checkpoints
- Sign-off Criteria for Sample Acceptance
- Confirm Next Steps & Validation Check
- Prioritize Categories by Consequence
- Define Acceptance Thresholds
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Solution Scope
Define the trial scope (2–3 categories for 4–6 weeks), sample shipments, quality specs, audit and certification requirements, pricing, and measurable acceptance criteria (fill rate, quality score, shelf life).
Scope Configuration
- Temperature-controlled receiving and quality inspection
- Ethylene-managed banana and avocado ripening
- Custom repacking, weighing, and case labeling
- USDA grade sorting and compliance stamping
- Case-level traceability tagging and lot capture
- Multi-temperature delivery with real-time monitoring
- Split-case and pallet pick-and-pack fulfillment
- Automated replenishment order fulfillment from POS
- Cold-chain temperature logging and compliance reports
- Bridge sourcing shipments during season transitions
- Food-safety recall retrieval and documentation
- Organic and specialty crop segregation and handling
- On-truck proof-of-delivery and condition verification
Scope
Temperature-controlled receiving and quality inspection
- What receiving temperature ranges must be maintained at dock and in staging (specify min/max °F or °C)?
- What are your expected daily/weekly case volumes for the trial categories?
- Which inspection checkpoints do you require (select all that apply)?
- What quality acceptance criteria should receiving use (e.g., % acceptable, defect thresholds, visual defects allowed)?
- Do you require quarantine/hold procedures and notification SLAs for failed shipments?
- Are there any facility or auditor access requirements during receiving (e.g., third-party auditors, buyer QA visits)?
Ethylene-managed banana and avocado ripening
- Which ripening profiles do you require for each SKU (e.g., green, break, ripe, firm-ripe)?
- What target shelf-life (days) on receipt do you expect for ripened product?
- Do you require ethylene dosing logs and batch-level ripening documentation?
- How many pallet positions and average pallet size should we reserve for ripening during the trial?
- Are there temperature or humidity constraints specific to your varieties (provide details if unusual)?
- Do you require custom ripening tests (e.g., Brix, firmness) before release?
Custom repacking, weighing, and case labeling
- Which SKUs need repacking or custom pack sizes for the trial?
- Do you require specific case weights, counts, or piece counts per pack?
- What labeling elements are mandatory (e.g., PLU, lot code, pack date, grower, country of origin)?
- Do you need pre-printed branded labels, GS1 barcodes, or custom artwork approval workflows?
- Are there target throughput or cut-off times for repack operations tied to delivery windows?
- Do you require tare/zeroing certification or scale calibration documentation for weighing?
USDA grade sorting and compliance stamping
- Which USDA grades are acceptable for each trial SKU (select all that apply)?
- Do you require physical grade sorting at packing or acceptance based on supplier certificates only?
- What stamping or compliance marks must appear on cases or pallets?
- What defect tolerance (e.g., % by count or by weight) is acceptable per shipment?
- Do you require certification copies (e.g., USDA AMS, state inspectors) before acceptance?
- Would you like photo documentation of sorted lots and stamped cases for audit trails?
Case-level traceability tagging and lot capture
- What case-level data elements must be captured (select all that apply)?
- Do you require GS1-128 or other barcode standards on every case?
- What is the maximum time allowed to retrieve traceability records during an inquiry?
- Will you need integration of case-level data into your traceability or ERP system?
- Do you need tamper-evident or RFID tagging for high-value SKUs?
- Are there retention requirements for traceability records (e.g., 2 years)?
Multi-temperature delivery with real-time monitoring
- Which temperature zones are required on truck (select all that apply)?
- Do you require real-time temperature telemetry and alerts during transit?
- What delivery window SLAs must drivers meet (e.g., appointment times, on-time %)?
- Do you require temperature certificates and route reports to be attached to invoices?
- Are there special handling instructions for mixed-temp loads at your dock?
- Do you need chain-of-custody proof (signed handoffs) at each delivery point?
Split-case and pallet pick-and-pack fulfillment
- Will you need split-case quantities (individual cases/units) rather than full pallet only?
- What pick frequency do you expect (daily, multiple times per day, weekly)?
- Do you require kitting or pre-assembled display packs as part of pick-and-pack?
- What accuracy target do you require for picks (% correct cases/units)?
- Are there label or invoice requirements per split-case (e.g., internal pick slips, customer-specific tags)?
- Do you require staging areas for split-case consolidation before loading?
Automated replenishment order fulfillment from POS
- Do you have POS data integration capability (real-time API, scheduled extracts, or none)?
- What reorder parameters do you want applied (min/max, par levels, ON-ORDER buffer)?
- Which SKUs should be included in automated replenishment for the trial?
- Do you require cadence for review/override of automated orders (daily, weekly)?
- Are there promotions or seasonality rules that should be excluded from automation?
- Do you require specific service-level fill-rate targets for automated fulfillment?
Cold-chain temperature logging and compliance reports
- What frequency of temperature logging do you require (per minute, per 5 minutes, per hour)?
- Which report formats and delivery methods do you need (PDF, CSV, API push)?
- What are your compliance thresholds and alarm tolerances for temperature excursions?
- Do you require automated compliance certificates attached to shipment records?
- How long should temperature logs be retained and made accessible?
- Do you require monthly/quarterly summaries for audits and regulatory reviews?
Bridge sourcing shipments during season transitions
- Which categories require bridging during transition periods (list SKUs)?
- Do you prefer domestic alternative suppliers, international sourcing, or a hybrid approach?
- What lead-time flexibility is acceptable for bridged shipments?
- Are there quality or origin constraints during bridge sourcing (e.g., no certain origins, organic-only)?
- Do you require pre-approved alternate suppliers or on-the-fly sourcing with buyer approval?
- What visibility and frequency of status updates do you need through the transition?
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Mutual Commit
Confirm commercial terms, SLA thresholds, approval gates, escalation paths, and the decision criteria to expand beyond the trial.
Agreement Modules
- Statement of Work (SOW)
- Commercial Terms & Pricing Schedule
- Service Level Agreement (SLA) and Performance Targets
- Trial Acceptance Criteria & Metrics
- Approval Gates & Expansion Decision Criteria
- Escalation Path & Contact Matrix
- Quality & Food Safety Commitments
- Sample Shipment & QC Protocol
- Logistics & Delivery Agreement
- Data Integration & Access Agreement
- Pricing, Invoicing & Payment Terms
- Recall & Liability Procedures
- Change Order & Scope Amendment Process
- Confidentiality & Non-Disclosure Agreement (NDA)
- Termination, Renewal & Post-Trial Transition
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Deployment
Schedule and execute onboarding tasks—facility audits, sample shipments, EDI/POS or replenishment integration, routing, and operational checkpoints with clear owners and timelines.
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Success
Validate trial results against agreed metrics, document findings for scale, and maintain a shared channel for issues, recalls, and continuous assortment optimization.
Success Reviews
- Trial Validation Review
- Exception & Root Cause Workshop
- Scale Recommendation & Commercial Commit
- Operational Handover & Shared Channel Setup
- Continuous Assortment Optimization Workshop
Meetings
- Create and populate the shared channel with named contacts and role tags.
- Identify root causes for high-priority exceptions with cross-functional agreement.
- Define corrective and preventive actions with clear owners and measurable verification.
- Set a time-bound verification cadence that satisfies the customer's QA and procurement teams.
- Execute corrective actions (update SOPs, route/pack changes) and log completion evidence.
- Schedule and run verification shipments and capture QC + temperature data for review.
- Update shared incident register and notify escalation contacts if recurrence occurs.
- Recap Trial Validation Outcome
- Secure commercial agreement to scale with documented pricing and SLA obligations.
- Define operational ramp timeline and measurable decision gates for phased expansion.
- Identify required approvals and owner responsible for contract execution.
- Draft contract addendum or SOW reflecting pricing, SLAs, and ramp schedule for legal review.
- Publish rollout timeline and communicate to operations, logistics, and merchant teams.
- Set a governance cadence for early-scale monitoring (weekly for first 30 days, then bi-weekly).
- Operational Handover Checklist
- Establish a live shared channel for day-to-day issues, escalations, and recall coordination.
- Agree explicit escalation paths and recall responsibilities with SLA timers.
- Ensure operations teams have data access and are scheduled for necessary training.
- Welcome & Objectives
- Publish the recall protocol and run the first tabletop exercise within 30 days.
- Grant dashboard access to buyer and operations stakeholders and confirm data feed integrity.
- Trial Learnings Recap & Demand Signals
- Define a prioritized set of experiments to improve fill rate, reduce shrink, and extend shelf life.
- Agree on measurement criteria and reporting cadence to evaluate experiment outcomes.
- Assign owners and timelines for pilots and ensure necessary data access for evaluation.
- Publish the optimization calendar with experiments, owners, and KPIs.
- Enable POS and QC dashboard views for experiment monitoring and share access.
- Run initial pilot(s) and collect required data packets for the next optimization review.
- Verify trial outcomes against each agreed acceptance metric and document evidence.
- Achieve a clear decision (accept, remediate+accept, extend, or reject) with owners and deadlines.
- Capture a concise executive summary of findings for stakeholder review.
- Produce consolidated Trial Results Report (data, photos, traceability pulls) for stakeholders.
- If remediation required, create Corrective Action Plan with owners, timelines, and verification metrics.
- Schedule follow-up validation checkpoint (date & owners) to verify corrective actions.
- Incident Packet Review (pre-worked)
- Restate Trial Scope & Acceptance Criteria
- Root Cause Analysis (5 Whys / Fishbone)
- Seasonal Sourcing & Transition Plans
- Shared Channel & Roles
- Scale Volume & Assortment Proposal
- Escalation Path & SLA Breach Flow
- Optimization Hypotheses & Experiments
- Current State Snapshot (What happened?)
- Pricing, Margins & Commercial Terms
- Impact Quantification
- SLA Thresholds & Penalties
- Corrective & Preventive Actions
- Measurement & Reporting Cadence
- Recall Response Protocol & Tabletop Triggers
- Consequence Assessment (What it cost/impacted)
- Decision Gates, Timeline & Expansion Criteria
- Data & Dashboard Access
- Pilot Planning & Owner Assignment
- Proof Points: Data & Artifacts
- Owner Assignment & Verification Plan
- Gap Summary & Root Causes (brief)
- Approvals & Contract Path
- Training & SOP Distribution
- Follow-up Cadence
- Wrap-up & Next Meeting