Facility Design & Technology
A Sealed Glass Venlo Greenhouse Engineered for Pharmaceutical Cannabis
Independent climate zones. Precision environmental controls. Pharmaceutical-grade post-harvest processing.
“We did not design a greenhouse and then ask how to make it pharmaceutical. We started with pharmaceutical requirements and designed the greenhouse around them.”
Facility Specifications
Pharmaceutical-Grade Infrastructure
Designed Plant Capacity
Designed Annual Capacity
Target Monthly Capacity
Designed Harvest Cycles
Structure
Sealed Glass Venlo
Dutch-engineered sealed glass greenhouse technology — the pharmaceutical standard for controlled environment cultivation. Eliminates contamination vectors while maximising natural light transmission.
Configuration
4 + 1 Independent Bays
Four flowering bays plus one vegetation bay, each designed for independent climate control. Engineered to enable staggered harvesting and chemovar-specific environmental optimisation.
Harvest Cycles
5–6 Per Year
Staggered harvesting across independent bays designed to ensure continuous production — 5 cycles in Year 1, scaling to 6 cycles from Year 2 onward.
Compliance
EU-GMP Designed from Blueprint
Engineered from blueprint to meet EU-GMP and GACP standards — not retrofitted. Every surface, workflow, and system architected for pharmaceutical-grade output.
Climate Control & Monitoring
Every Variable. Every Bay. By Design.
Every environmental variable — temperature, humidity, CO₂, light intensity, airflow — is designed for independent control and continuous monitoring across each cultivation bay. Sealed Venlo greenhouse technology engineered to create a pharmaceutical-grade controlled environment that eliminates contamination risk while optimising plant performance.
Temperature
23–28°C
Per-bay precision control, designed for growth-stage adjustment
Light (PAR)
400–1200 µmol/m²/s
Natural + supplemental lighting with photoperiod scheduling
Humidity
45–65% RH
VPD-driven control designed to optimise transpiration and resin production
CO₂
800–1500 ppm
Enrichment during photosynthesis hours for enhanced yield
Airflow
Positive pressure
HEPA-filtered circulation engineered to prevent pathogen ingress
Irrigation
Automated fertigation
Nutrient-specific dosing designed for growth-phase and chemovar calibration
Staggered Harvesting
Different bays at different growth stages simultaneously — enabling continuous production with no seasonal gaps.
Chemovar-Specific Optimisation
Each bay runs independent environmental protocols tailored to the specific chemovar being cultivated.
Contamination Isolation
Sealed bay separation so one bay's issue cannot affect others — pharmaceutical-grade containment.
Year-Round Production
Staggered cycles deliver 5–6 harvests per year, ensuring consistent supply for distribution partners.
Technology Stack
Environmental Control Platform
Five integrated technology layers engineered to work in concert, maintaining pharmaceutical-grade environmental conditions. Every parameter designed to be monitored, logged, and traceable to EU-GMP standards.
Environmental Sensors
Designed for continuous multi-point monitoring across every bay with sub-minute sampling intervals.
- —Temperature & humidity probes
- —VPD calculation modules
- —CO₂ concentration meters
- —PAR light level sensors
- —Substrate moisture sensors
Automated HVAC
Sealed environment management engineered to ensure pharmaceutical-grade air quality and contamination prevention.
- —Independent per-bay climate loops
- —HEPA-filtered air handling
- —Positive pressure management
- —Automated vent and shade control
- —Emergency override protocols
Irrigation & Fertigation
Precision nutrient delivery designed and calibrated for growth-phase and chemovar-specific requirements.
- —Automated nutrient dosing
- —pH and EC monitoring
- —Growth-phase nutrient profiles
- —Runoff analysis and recirculation
- —Water quality management
Data Logging & Trending
Designed for complete environmental traceability, linking every batch to its cultivation conditions — essential for EU-GMP documentation.
- —Historical environmental data archive
- —Batch-correlated environmental records
- —Deviation alerts and notifications
- —Trend analysis dashboards
- —EU-GMP compliant audit trails
IPM Monitoring
Integrated pest management designed to operate within pharmaceutical compliance — targeting zero synthetic pesticide residues on final product.
- —Sticky trap monitoring network
- —Beneficial insect deployment
- —Environmental condition tracking
- —Preventive treatment scheduling
- —Incident logging and CAPA
Cultivation Process
Seed-to-Shipment: Eight Pharmaceutical-Grade Steps
From genetics selection to export packaging, every step in our cultivation process is designed to meet EU-GMP pharmaceutical standards. Each stage is monitored, documented, and traceable — ensuring consistent, compliant product in every batch.
Step 01 of 08
Genetics Selection
Sourcing and selecting high-quality cultivars with documented lineage and consistent cannabinoid and terpene profiles. Every chemovar in our portfolio is chosen for pharmaceutical-grade reproducibility.
Step 02 of 08
Propagation
Clonal propagation from mother plants ensuring genetic consistency across every production batch. Each clone is an identical copy, guaranteeing batch-to-batch uniformity in cannabinoid composition.
Step 03 of 08
Vegetation
Controlled vegetative growth in a dedicated bay with optimised photoperiod, nutrition, and environmental conditions. Plants develop the structural foundation for maximum flowering potential.
Step 04 of 08
Flowering
Transfer to independent flowering bays with chemovar-specific light, temperature, and humidity protocols. Each bay is designed as an isolated environment optimised for the specific cultivar.
Step 05 of 08
Harvest
Precisely timed harvest based on trichome maturity assessment and cannabinoid analysis. Every plant is evaluated individually to ensure peak potency and terpene expression at the moment of harvest.
Step 06 of 08
Drying & Curing
Controlled drying and curing in pharmaceutical-grade conditions to preserve terpene profiles and ensure consistent moisture content. Temperature and humidity are precisely regulated throughout.
Step 07 of 08
Testing & Quality Assurance
Full analytical testing suite ensuring every batch meets European pharmaceutical standards. No product will leave the facility without a complete Certificate of Analysis.
Step 08 of 08
Packaging & Export
Pharmaceutical-grade packaging meeting EU import requirements, with full batch documentation and Certificate of Analysis. Every shipment is export-ready with complete regulatory documentation.
Step 01
Genetics Selection
1 / 8 steps
Genetics Selection
Sourcing and selecting high-quality cultivars with documented lineage and consistent cannabinoid and terpene profiles. Every chemovar in our portfolio is chosen for pharmaceutical-grade reproducibility.
Propagation
Clonal propagation from mother plants ensuring genetic consistency across every production batch. Each clone is an identical copy, guaranteeing batch-to-batch uniformity in cannabinoid composition.
Vegetation
Controlled vegetative growth in a dedicated bay with optimised photoperiod, nutrition, and environmental conditions. Plants develop the structural foundation for maximum flowering potential.
Flowering
Transfer to independent flowering bays with chemovar-specific light, temperature, and humidity protocols. Each bay is designed as an isolated environment optimised for the specific cultivar.
Harvest
Precisely timed harvest based on trichome maturity assessment and cannabinoid analysis. Every plant is evaluated individually to ensure peak potency and terpene expression at the moment of harvest.
Drying & Curing
Controlled drying and curing in pharmaceutical-grade conditions to preserve terpene profiles and ensure consistent moisture content. Temperature and humidity are precisely regulated throughout.
Testing & Quality Assurance
Full analytical testing suite ensuring every batch meets European pharmaceutical standards. No product will leave the facility without a complete Certificate of Analysis.
Packaging & Export
Pharmaceutical-grade packaging meeting EU import requirements, with full batch documentation and Certificate of Analysis. Every shipment is export-ready with complete regulatory documentation.
