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Food regulatory and quality services.

Choose the Regulatory Horizon Tracker, label review, QMS/SQF support, or launch readiness. Each service has a written scope, deliverables, timeline, and price or quote.

Program 01 · Subscription

Regulatory Horizon Tracker

Monitor FDA, USDA, FTC, TTB, and state food-regulatory developments in one maintained tracker. Sources are checked daily, and material changes are reviewed before publication.

Labeling: allergens, ingredient statements, nutrition facts, front-of-pack, country-of-origin
Packaging & materials: PFAS bans, EPR laws, recycled-content mandates, state packaging bills
Ingredients & additives: color-additive rules, synthetic-dye phase-outs, GRAS reform
Claims: health, structure-function, “natural” and bioengineered disclosure, environmental marketing
Contaminants & substantiation: heavy metals, PFAS in food, methods of analysis, enforcement-posture changes
Traceability & inspection: FSMA §204, preventive controls, USDA FSIS swine and poultry inspection-system rules (NSIS/NPIS), USDA-inspected eligibility

Plus state legislative activity and emerging categories (cultivated meat, plant-based, novel ingredients).

Founding Access
$399/mo

1 named user · available now

Organization Pilot
Scoped access

Defined workflow, controls, and success criteria

See full pricing
Program 02 · Per-project

Label Compliance Review

Review of one label against FDA, USDA, FTC, and applicable state requirements. You receive marked-up artwork and a written report within 5 business days. A 2-business-day rush review is available.

Full FDA (CFSAN), USDA AMS + FSIS, FTC, state-level requirements
Nutrition facts verification, allergen statements, claims review
Packaging copy and on-pack graphic compliance
Redline markup + written compliance report
30-day follow-up support
$499/SKU 3-pack $1,297 · 10-pack $3,990 · rush +$250
See the full review scope Request a review
5-day review path
1

Day 1 · Intake

Submit labels, ingredients, claims, and packaging files.

2

Days 2–4 · Review

Review labeling, claims, allergens, nutrition information, and applicable federal and state requirements.

3

Day 5 · Deliver

Receive marked-up artwork and a written report with required changes and open questions.

30-day support

Follow-up questions on findings, included in every review.

Program 03 · Inquiry-based

QMS / SQF Support

Get help preparing for SQF, BRCGS, FSSC 22000, HACCP, and PCQI reviews. Work is delivered remotely through document review and live sessions.

Readiness Assessment

Remote document review against SQF, BRCGS, FSSC 22000, or GMP. Gap analysis with prioritized action plan.

1–2 weeks

Schedule a consultation

Audit Prep Program

Review and update SOPs, HACCP/PCQI plans, forms, and audit records. Includes a virtual mock audit and pre-audit coaching.

4–8 weeks

Schedule a consultation

QMS Partnership

Quarterly document reviews, regulatory-impact reviews, virtual mock audits, and training. Tracker access is separate.

Ongoing monthly

Schedule a consultation

SQF Edition 10 transition: audits anticipated to begin no earlier than January 2, 2027 (per SQFI; contingent on GFSI benchmarking). Readiness Assessment fee can be credited toward Audit Prep if you convert within 30 days.

Program 04 · Advisory

Launch Readiness

For new products or expansion into new channels or states. Mirelis reviews the requirements and identifies the changes needed before launch.

Launch Review

Review ingredients, claims, label copy, and state requirements before a new product launches.

2–4 weeks

Schedule a consultation

Market Expansion

Review an existing product for a new state or sales channel. You receive a list of label, product, and documentation changes needed for that market.

1–3 weeks

Schedule a consultation

How client files are handled.

The public Tracker does not require label, formulation, or supplier uploads. Consulting files are requested only after scope and confidentiality terms are agreed.

Read the privacy and confidentiality summary

Before you send files

Mirelis confirms the files needed, the transfer method, and any confidentiality requirements.

Access is limited

Administrative and technical controls limit access and reduce unnecessary exposure.

Requirements are written down

Any special storage, transfer, retention, or deletion terms are included in the engagement documents.

Request a consultation.

Share the product, deadline, and work you need. Mirelis will confirm fit and provide the next step.

Start an inquiry View pricing