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Protocol Raw — Founder's Action Guide

What this document is: Your "start here" guide to getting Protocol Raw manufactured. Plain English, action-focused.

What this document is NOT: Technical specifications (those exist separately when you need them).


Part 1: How the Supply Chain Works

The Simple Version

You don't manufacture dog food. You don't blend powders. You don't weigh micro-ingredients before every batch.

You control the specs. Others do the physical work.

Here's the model:

┌─────────────────────────────────────────────────────────────────────┐
│                                                                     │
│   YOU (Protocol Raw)                                                │
│   • Set specifications                                              │
│   • Approve COAs (certificates of analysis)                         │
│   • Manage relationships                                            │
│   • Audit occasionally                                              │
│                                                                     │
└─────────────────────┬───────────────────────────────────────────────┘
                      │ You send: Pack specs + approved supplier list
                      │ They send: COAs for approval, then finished packs
┌─────────────────────────────────────────────────────────────────────┐
│                                                                     │
│   BLENDER/PACKER                                                    │
│   • Sources kelp, oyster powder, mussel powder, CLO                │
│   • Checks COAs against your specs                                  │
│   • Blends Dry Functional Pack                                      │
│   • Produces batch-dose Functional Preblend units (bags/drums/totes)│
│   • Bottles Oil Pack (CLO) in batch doses                           │
│   • Ships directly to co-packer (or to you if you prefer)           │
│                                                                     │
└─────────────────────┬───────────────────────────────────────────────┘
                      │ They send: Labelled preblend units + bottles (with lot numbers)
┌─────────────────────────────────────────────────────────────────────┐
│                                                                     │
│   CO-PACKER                                                         │
│   • Sources meat, organs, eggs, commodity oils (fish oil, flax)     │
│   • Receives your Functional Preblend + Oil Pack (lot-tracked)      │
│   • Grinds, mixes, adds preblend, portions into 500g trays          │
│   • Seals (MAP), labels, freezes, holds for your lab clearance      │
│   • Ships to you or your 3PL                                        │
│                                                                     │
└─────────────────────────────────────────────────────────────────────┘

Why This Model?

The problem: Your formulation uses COA-controlled anchors (kelp for iodine, oyster for zinc, mussel for manganese, CLO for vitamin D). These need verified potency to hit FEDIAF compliance. If you let the co-packer source random kelp powder, you lose control.

The solution: You control the critical micro-ingredients through a blender/packer who makes standardised Functional Preblend units. The co-packer just adds the preblend — they don't need micro-scales or nutritionist knowledge.

Your ongoing work: Approve COAs when lots change (maybe monthly), audit annually, handle exceptions. Not daily/weekly operational work.


Part 2: Decisions You Need to Make First

Before you contact anyone, decide these:

Decision 1: Standard Batch Sizes

Pick 1-2 batch sizes and stick to them. This makes everything simpler and cheaper.

Phase Recommended Batch Size Why
Phase A (months 1-6) 1,000 kg Balances testing cost, MOQs, risk
Phase B (months 7-18) 2,500 kg Volume efficiency
Phase C (scale) 10,000–20,000+ kg Co-packer run efficiency + fewer lot-change events

Your decision: __ kg (Phase A), _ kg (Phase B), and ___ kg (Phase C)

Once set, your Functional Preblend units are made in these exact batch doses. No weighing or math at the co-packer.

Note: At Phase C, "one sachet per batch" becomes "one preblend unit per batch" (e.g., 25kg bags, drums, or totes), still lot-tracked and COA-controlled.

Decision 2: Who Holds Functional Pack Inventory?

Option How it works Best for
A: Blender ships to co-packer You never touch the preblend units. Blender ships directly when co-packer orders a batch. Least hassle. Recommended.
B: You hold inventory Blender ships preblend units to you. You ship to co-packer per batch. More control, more work.
C: Co-packer holds inventory Blender ships bulk preblend units to co-packer. Co-packer stores and uses as needed. Works if co-packer has space and you trust them.

Recommendation: Option A for simplicity. You're not in the warehousing business.

Your decision: Option ___

Decision 3: Who Sources Anchor Ingredients?

Option How it works Best for
Blender sources to your spec You give them specs + approved supplier list. They buy, check COAs, reject if out of spec. Recommended. Less work for you.
You source, blender just blends You buy kelp/oyster/mussel/CLO, ship to blender, they make preblend units. More control, more cash flow/logistics burden.

Recommendation: Let the blender source. You approve suppliers and COA specs upfront. They execute.

Your decision: Blender sources / You source (circle one)

Decision 4: Oil Pack Contents

The Dry Pack is straightforward (anchors + carriers/fibre in a COA-controlled Functional Preblend).

For oils, decide:

Option Oil Pack contains Co-packer sources
A: CLO only in Oil Pack Just cod liver oil (vitamin D anchor) Fish oil + flaxseed oil
B: All oils in Oil Pack CLO + fish oil + flaxseed Nothing — all oils come from you

Recommendation: Option A. CLO is the critical one (vitamin D). Fish oil and flaxseed are commodity — let the co-packer source them to a simple spec (e.g., "salmon/sardine oil, EPA+DHA ≥25%, peroxide <5").

Your decision: Option ___

Decision 5: Stool Stability System (Whole-Food Fibre)

Your target customer is family pets and kibble switchers. To make stool issues unlikely at scale, you will include a small whole-food fibre system inside the Functional Preblend.

Default recommendation (finished-product inclusion targets): - Pumpkin powder or carrot fibre: ~2.0% - Psyllium husk: ~0.5% - Nutritional yeast: reduced (e.g., ~3.0%) as carrier/B-vitamin support, not the dominant dry mass

Why it matters: This reduces loose-stool tickets during transition without using synthetic additives.

Your decision: - Fibre source: Pumpkin powder / Carrot fibre (circle one) - Psyllium: Yes / No - Label naming: "psyllium husk", "pumpkin powder" / "carrot fibre" (confirm)


Part 3: The Action Sequence

Here's what you do, in order.

Phase 0: Home Pilot (Weeks 1-4)

You do this yourself to validate the formulation before spending money on commercial partners.

Week Action
1 Source pilot ingredients (10kg quantities) from retail/online
1 Get COAs for anchor ingredients if possible (or just use reputable brands)
2 Run 10kg home pilot batch (see Home Pilot Protocol)
2 Submit composite sample to UKAS lab for full nutritional panel
3-4 Receive results
4 DECISION GATE A: FEDIAF compliant on lab panel? If yes → proceed. If no → adjust and re-run.
4 DECISION GATE B: GI tolerance acceptable on transition test (stool scoring)? If yes → proceed. If no → adjust (usually fibre/fat variability) and re-run.

GI tolerance test (simple): - Use a 7–10 day transition from kibble → Protocol Raw - Track stool score daily (and gas/itch notes) - Pass = no persistent diarrhea/urgency in the test group after transition

Output: Lab report proving your formulation works + GI tolerance data confirming stool stability.


Phase 1: Find Your Blender/Packer (Weeks 2-6)

Can run parallel to home pilot.

Week Action
2 Write Pack Specification Sheet (use template in your doc pack)
2-3 Identify 3-5 UK blender/packers (see "Where to Find Them" below)
3 Send RFQ with your Pack Spec Sheet
4-5 Receive quotes, ask clarifying questions
5-6 Select blender/packer, agree terms
6 DECISION GATE: Blender/packer confirmed? If yes → proceed to co-packer.

What you're asking them: - "Can you source these ingredients to these specs?" - "Can you blend the Dry Pack and portion into X kg batch-dose Functional Preblend units?" - "Can you bottle CLO in X kg batch doses?" - "What's the lead time and MOQ?" - "Will you send me COAs for approval before production?"

Where to find blender/packers: - UK feed/pet supplement blenders (search "pet food premix UK", "feed supplement blending UK") - Contract packing companies that handle powders - Ask your co-packer candidates — they often know blenders they've worked with - Jamie's FMCG network may have leads


Phase 2: Find Your Co-Packer (Weeks 4-10)

Start this once you have lab validation and blender/packer lined up.

Week Action
4-5 Send Co-Packer RFQ to 4-6 candidates
5-7 Receive quotes, classify using capability checklist
7-8 Site visits to top 2-3
8-9 Negotiate terms, confirm they'll accept your Functional Preblend units
9-10 Sign agreement
10 DECISION GATE: Co-packer confirmed? If yes → schedule first batch.

What you're asking them: - "Can you run this formula?" (give them the Production Master Spec) - "Can you add pre-made Functional Preblend units at the mixing stage and record lot numbers?" - "Do you have quarantine capacity for hold-and-release?" - "What's your price at 1,000 kg / 2,500 kg / 5,000 kg batches?"

What you're NOT asking them: - To source micro-ingredients (that's the blender/packer's job) - To weigh powders on micro-scales (that's done for them) - To understand FEDIAF compliance (that's your job)


Phase 3: First Commercial Batch (Weeks 10-14)

Week Action
10 Order Functional Preblend from blender (allow 2-3 week lead time)
10 Confirm co-packer production slot
11-12 Blender ships Functional Preblend to co-packer
12-13 Co-packer runs first batch (1,000 kg): grinds, mixes, adds preblend + oils, fills 500g trays, MAP-seals, labels, freezes
13 Co-packer sends samples to lab (pathogen panel)
13 Batch sits in quarantine (HOLD)
13-14 Lab results received
14 DECISION GATE: Pathogens clear? If yes → release batch. If no → destroy, investigate.
14 First customer shipments

Part 4: What's Ongoing vs One-Time?

One-Time Setup Work

Task When Time Required
Run home pilot, get lab validation Weeks 1-4 10-15 hours
Find and contract blender/packer Weeks 2-6 5-10 hours
Find and contract co-packer Weeks 4-10 15-25 hours (including site visits)
Set up batch tracking in your systems Week 10 Already done (SOP 01)

Ongoing Work at Scale

Task Frequency Time Required
Review/approve COAs from blender When ingredient lots change (monthly-ish) 15-30 mins
Trigger batch production (tell co-packer to run) Per batch (weekly at scale) 5 mins (email/call)
Enter batch in system when co-packer confirms Per batch 30 seconds (your ops portal)
Review pathogen results, release batch Per batch 2 mins (automated, you just confirm)
Audit blender/packer Annually Half day
Audit co-packer Annually Half day

The key point: Once set up, your per-batch work is minimal. The system you've already built (SOP 00, 01, 02, etc.) handles most of it automatically.


Part 5: What Could Go Wrong (and What to Do)

Problem: Blender/packer COA shows anchor ingredient out of spec

Example: Kelp iodine is 600 mg/kg instead of your spec'd 800-1200 mg/kg.

Action: Reject that lot. Tell blender to source compliant lot before making your preblend units.

Your exposure: Delay of 1-2 weeks while they source new kelp. No product goes out wrong.


Problem: Co-packer can't/won't add preblend properly

Example: They mix up lot numbers, or add preblend at the wrong stage.

Action: This is why you do a site visit and watch the first batch. Build clear instructions. If they can't follow them, find a different co-packer.


Problem: First batch fails pathogen test

Example: Salmonella detected.

Action: Destroy batch. Do NOT release. Investigate with co-packer (ingredient source? cross-contamination? temperature abuse?). Fix root cause. Run new batch.

Your exposure: Cost of one batch (~£4,000-5,000 at 1,000 kg). But your proof system is intact — you caught it before it reached customers.


Problem: Lab results show nutritional miss (e.g., iodine low)

Example: Routine audit shows iodine at 280 µg/1000 kcal vs FEDIAF minimum 350 µg.

Action: Check kelp lot COA — did potency drop? Adjust preblend formula: increase kelp weight proportionally. Future batches will be compliant.

Your exposure: A batch labelled "Complete" must meet the standard it claims.

Action: If a batch misses a FEDIAF minimum, do not release as "complete." Hold the batch, investigate root cause, and decide corrective action (rework/blend-down/relabel/dispose) with your nutrition/regulatory sign-off. Fix going forward via preblend adjustment.


Problem: Fibre ingredients introduce contamination risk or processing issues (pumpkin/carrot fibre, psyllium)

Risk: Plant powders can carry higher baseline microbial load and may cause clumping if not dispersed correctly (psyllium gels fast).

Action: - Require COAs + acceptance criteria for fibre ingredients (micro + contaminants) in your Supplier Spec Pack - Validate dispersion on first commercial batch (visual check + sampling) - If clumping occurs: adjust mixing sequence (preblend into a meat masterbatch first), mixing time, and temperature control


Part 6: Quick Reference - Who Does What

Task You Blender/Packer Co-Packer
Set ingredient specs
Source anchor ingredients (kelp, oyster, mussel, CLO)
Check anchor COAs against spec Approve ✓ Execute
Produce Functional Preblend (anchors + carrier + fibre)
Portion into batch-dose preblend units (bags/drums/totes)
Bottle CLO in batch doses
Ship Functional Packs to co-packer Receive
Source meat, organs, eggs, commodity oils
Grind, mix, add preblend + oils, fill trays, seal (MAP), label
Record Functional Pack lot numbers
Freeze and hold in quarantine
Submit samples for pathogen testing ✓ (or you)
Review pathogen results, release batch
Ship to customers / 3PL ✓ (or you in Phase A)

Part 7: Documents You'll Use

Document What it's for When you use it
Pack Specification Sheet RFQ to blender/packers Finding your blender/packer
Supplier Spec Pack Tells blender what COA fields to check Give to blender once contracted
Production Master Spec Full formula + processing instructions Give to co-packer
Co-Packer RFQ Capability checklist + pricing template Finding your co-packer
Home Pilot Protocol Step-by-step 10kg trial batch Your home pilot (Phase 0)
Lab Validation Panel What tests to request from lab Submitting pilot + ongoing batches

Your Next Steps

Right now: 1. Confirm your batch size decisions (1,000 kg Phase A / 2,500 kg Phase B / 10,000–20,000+ kg Phase C recommended) 2. Confirm inventory model (blender ships direct to co-packer recommended) 3. Confirm oil pack contents (CLO only recommended) 4. Confirm stool stability system (fibre source + psyllium)

This week: 1. Start sourcing 10kg pilot ingredients 2. Identify 3-5 blender/packer candidates 3. Identify 4-6 co-packer candidates (Jamie may have leads)

Next prompt: I'll create the Pack Specification Sheet you'll send to blender/packers.


Document Control

Field Value
Document Founder's Action Guide
Version 1.1
Created January 2026
Updated February 2026
Owner Anton
Classification INTERNAL