Designed for Canada.
Built for Europe.

We specialize in cannabis regulatory consulting, including licensing strategy, compliance frameworks, SOP development, facility planning, audit readiness, and operational execution support in regulated markets such as Canada and Europe.

Cannabis regulations are complex and constantly evolving. Regulators assess execution, not intent. A consulting partner helps you structure compliant documentation and systems (including SOPs) that withstand audits and inspections efficiently.

We support applications for all major Canadian licences including micro-cultivation, standard cultivation, processing, and ancillary licences, ensuring full compliance with Health Canada's licensing requirements.

A Standard Operating Procedure (SOP) is a documented set of instructions describing how critical processes should be performed. High-quality SOPs are essential for GPP (Good Production Practices), audit readiness, and operational consistency.

GPP (Good Production Practices): Canadian cannabis production standards under Health Canada.

GACP (Good Agricultural and Collection Practices): European standards for cultivation and harvesting of medicinal plants.

GMP (Good Manufacturing Practices): Quality practices for reliable production.

EU-GMP: The European pharmaceutical standard required for medicinal cannabis manufacturing and export.

Yes. We support growers and processors with EU-GMP readiness, including gap analysis, documentation systems, quality controls, and operational alignment to European regulatory expectations.

The process involves project planning, regulatory risk assessment, documentation preparation, SOPs, security planning, facility design, submission to Health Canada, and audit readiness. Our team manages all stages to increase approval success rates.

Audit readiness means your documentation, SOPs, training, and operations are aligned and defensible under inspection. Canadian and EU authorities inspect compliance at any time, and being prepared reduces risk of non-conformances.

Yes. Successful export requires understanding international quality standards, including EU-GMP compliance. We help design systems that meet export market requirements and improve competitive positioning globally.

Licensing timelines vary depending on licence type, completeness of documentation, and regulator schedules. Preparing quality SOPs, floor plans, and compliance systems speeds up review, but cannabis licensing typically spans several months.

Yes. We work with projects of all sizes — from micro-cultivation start-ups to larger LPs — as long as they are committed to regulatory rigor and operational discipline.

Cannabis consulting requires deep regulatory knowledge (Health Canada, GACP, GMP/EU-GMP), industry-specific experience, and an understanding of inspection behaviors and compliance risk — not just business planning.

Yes. Beyond licensing, we provide implementation support, compliance systems, SOP training, quality assurance planning, and ongoing operational strategy.

Yes. We audit existing SOPs and develop revised, audit-ready versions that are aligned with GPP, GACP, GMP, or EU-GMP expectations and tailored to your operational realities.

A gap analysis compares your current compliance systems against regulatory requirements (GPP, EU-GMP, etc.) to identify deficiencies and remediation needs before regulators review your files.

Yes. We provide compliant facility floor plans and security plan guidance that meet licensing requirements and support operational risk mitigation.

We serve clients in Canada and across Europe (including Germany, UK, Switzerland, emerging markets) with a focus on regulatory compliance, operational execution, and market readiness.

The first step is a Strategy Call — a structured 30-minute session to understand your project, assess feasibility, and identify regulatory risks and next steps.