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Cannabis compliance isn't just about passing inspections — it's about building operational systems that keep you compliant as a natural byproduct of doing things right. Multi-jurisdiction regulatory complexity, evolving state and local requirements, and the high cost of non-compliance make proactive compliance management essential to protecting your license, your operation, and your investment.
Regulatory violations in cannabis carry consequences that go far beyond fines. License suspension or revocation can shut down operations entirely. Product recalls destroy revenue and brand reputation. Failed inspections create operational disruption and legal exposure. In an industry where your license is your most valuable asset, compliance isn't overhead — it's insurance for everything you've built.
Facility compliance review and gap analysis identifying areas of regulatory risk before they become violations. Operational SOP development aligned with your specific state and local regulations, building compliance into daily workflows rather than treating it as a separate task. Documentation systems and record-keeping protocols that satisfy regulatory requirements while minimizing administrative burden on your team.
Audit preparation and mock inspections so your team knows exactly what to expect and how to perform under regulatory scrutiny. Multi-state compliance strategy for operators expanding across jurisdictions with different regulatory frameworks. Tribal cannabis regulatory support drawing on our direct experience with tribal cannabis program development. Ongoing regulatory monitoring keeping you informed of changes that affect your operation before they take effect.
Our approach treats compliance as a feature of well-run operations, not a separate cost center. When SOPs are designed correctly, they serve both compliance requirements and operational efficiency simultaneously. When training systems are built properly, they keep teams current on regulations while also improving cultivation consistency and quality. When documentation is structured intelligently, it satisfies inspectors while also providing the operational data you need to manage your business. Compliance done right makes your operation better, not just legal.
Whether you're preparing for an upcoming inspection, expanding into a new jurisdiction, or want to ensure your current operations meet all regulatory requirements, a compliance review is the starting point. We'll assess your current compliance posture, identify gaps and risks, and build a prioritized remediation plan. Contact Urth & Fyre at info@urthandfyre.com or use our contact form to schedule your review.
A test-driven, buyer-focused acceptance test checklist for used/reconditioned lab circulators and chillers—covering temperature stability under load, heat-up and pull-down performance, pump verification, leak checks, alarms, sensor validation, electrical draw, noise/vibration, and visual inspection—plus the most common commissioning pitfalls and how Urth & Fyre can deliver documented SAT results for production confidence.
In-process potency testing can speed decisions without creating a “shadow lab”—if you design it like a controlled, QA-owned decision-support system. This post lays out a practical release-support workflow (sampling, chain-of-custody-lite, daily system suitability, calibration/verification checks, defined use cases, and audit-ready documentation) and shows how a turnkey HPLC like Urth & Fyre’s Shimadzu Hemp/Cannabinoid Analyzer can fit into a governed operations environment.
Most net-contents headaches on high-speed packaging lines come from control latency: variable product flow meets slow feedback, creating either overweight giveaway or a spike in false rejects. This practical guide shows packaging managers how to design buffer capacity, set target weights versus tolerances, and use checkweigher data to tune a multihead weigher upstream—while calling out common failure modes like sticky product smearing, vibratory feeder drift, tare variability, and sloppy changeovers. Includes benchmarks, an easy-to-explain control-loop diagram, and SOP-ready steps for NTEP-appropriate verification and audit defense.
Micro-cracks and late-stage leaks in press-cap vapor devices are usually born from tiny misalignments, dimensional drift, contamination, and inconsistent force ramps—not “bad luck.” This practical guide shows packaging and QA managers how to build a daily routine around tray/fixture checks, first-article verification, force setpoint validation, and a simple destructive test cadence, with documentation patterns (URS/FAT/SAT-lite, training sign-offs) that make the process auditable and repeatable.
Choosing the right bath fluid is the fastest way to protect your high temperature circulator, hit reaction temperature under load, and avoid sludge, seal swell, and audit headaches. This guide breaks down viscosity, oxidation stability, flash/autoignition safety, materials compatibility, filtration, change intervals, and documentation—plus how to match fluid choice to circulator pump capability like the JULABO SL-12 (300°C, 12 L).
A repeatable 30-minute pre-shift cartridge filling setup routine for production supervisors—covering thermal equilibration, viscosity confirmation, needle selection, purge/prime, timed dose checks, and first-article approval—plus the failure modes and documentation practices that reduce rework and improve audit readiness. Includes a practical workflow for the Thompson Duke MCF1.
