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Pharmaceutical laboratory — clean analytical environment
Laboratory glassware and scientific research setup
GACP-certified supply · EU-grade docs · worldwide export·GACP certified

We are Verdant MedicalDocumented GACP Cannabis Supply

GACP-certified indoor cultivation across two Thai facilities with 5,000+ kg/year capacity. Consistent batches, full traceability, and export-ready documentation for importers, manufacturers, and pharmacies globally.

01/02
  • GACP Certified
  • Batch Traceability
  • Export documentation
  • Dual-Site Production
  • Global export ready

At a glance

Built for verified, scalable supply

Verdant Medical operates dual-site indoor operations, dedicated cultivar programs, and capacity aligned to international import volumes — starting from EU qualification expectations and extending to partners worldwide.

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Production Facilities

Bangkok & Pattaya

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Total footprint

Indoor

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kg / Year Capacity

Scalable production

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Program cultivars

Specification-driven

Specification-driven, not marketing-driven

Verdant Medical delivers measurable attributes, documented batches, and formats designed for import and manufacturing workflows in the EU and other regulated markets.

Dried Flower

Documented inflorescence across multiple cultivars. THC and CBD ranges documented per batch with full terpene profiling.

  • 18–24% THC range
  • Indoor
  • Batch-level COAs
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Bulk & Custom Formats

Packaging formats from bulk containers to pre-packed units. Labeling and documentation matched to destination market requirements.

  • Bulk 1–25 kg units
  • Pre-packed options
  • EU-compliant labeling
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Lab-backed testing
Cultivar traceability
Spec sheets on request

Why Thailand — operational edge for EU supply

Climate, genetics, flexibility, and unit economics — explained the way procurement and QA teams evaluate supply partners.

Indoor Climate Control

Fully indoor cultivation with closed-loop environmental control — not open-air tropical growing. Temperature, humidity, and irrigation are monitored and adjusted for repeatable batches and predictable planning.

Verified Genetics Programs

Cultivar selection and stability programs aligned to specification-driven buyers — not recreational markets.

Operational Flexibility

Batch sizing and production programs matched to importer and manufacturing workflows. Scale on demand.

Cost-Effective Production

Industrial production economics you can model — transparent pricing with lower overhead than European indoor facilities.

Lush green rice fields in Chiang Mai, Thailand — regional agricultural landscape
Clean room manufacturing facility — controlled production environment
Golden rice fields nestled between green hills in Chiang Mai, Thailand

Production footprint

Dual-site operations provide redundancy for batch planning and export scheduling — no single point of failure.

Bangkok Facility

2,000 m²

Main production, QA, export coordination

Pattaya Facility

1,500 m²

Supplementary capacity, cultivar programs

From cultivation to global delivery

Verdant Medical provides end-to-end visibility across every step — because buyers evaluate the full chain, not just the flower. EU qualification is our anchor; distribution can extend worldwide where regulations allow.

5,000+

kg/year capacity

Cultivation logs · Batch records

Step 1Cultivation

  • Dual-site GACP-certified facilities in Thailand
  • Documented genetics with full seed-to-harvest traceability
  • Controlled climate: temperature, humidity, and light logging
  • Disciplined harvest protocols with batch assignment at cut

Audit-ready, not "just trust us"

At Verdant Medical, every claim is backed by process documentation, accredited testing, and a clear paper trail designed for EU and international regulatory expectations.

GACP Certification

Good Agricultural and Collection Practices certification covering cultivation, harvesting, and post-harvest handling. Aligned to EU buyer due diligence requirements.

Certificate of Analysis

Batch-level COAs from accredited labs covering cannabinoid potency, terpene profile, heavy metals, pesticides, microbiology, and moisture content.

QP Release Support

Documentation structured to support Qualified Person release in destination markets. Chain-of-custody and batch linkage from cultivation through export.

Regulatory Pathway

Export permits, import license coordination, and regulatory context for each destination market. Structured to reduce compliance friction for partners.

Documentation pack includes

Batch production records
Stability data & storage conditions
Deviation & CAPA reports
Pesticide & contaminant panels
Method validation references
Export permit documentation

Structured collaboration — no guesswork

Verdant Medical offers a clear five-stage process from initial qualification to ongoing supply, so your procurement team can map our process to yours.

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Step 01

Qualification

Initial assessment of your requirements, volumes, documentation needs, and destination market specifics.

02
Step 02

Sample Evaluation

Representative samples with full COA pack for your internal testing, QP review, and specification confirmation.

03
Step 03

Onboarding

Formal agreement, documentation alignment, import/export permit coordination, and logistics setup.

04
Step 04

First Shipment

Production run to your specification with full batch documentation, quality release, and export coordination.

05
Step 05

Ongoing Supply

Regular production cycles, continuous improvement, expanded cultivar programs, and long-term volume planning.

Our facility and track record — as it actually looks.

On-site facility photography

Every photo is taken at our Bangkok and Pattaya cultivation sites. What you see reflects the actual conditions and scale behind every batch we ship.

Rows of cannabis plants in a controlled indoor environment
Cannabis flower close-up — documented bud detail
Cannabis flower close-up — indoor-grown CBD-dominant plant

Trusted by EU pharmaceutical buyers partnering with Verdant Medical

References from importers, manufacturers, and distributors who have completed our qualification process.

Verdant Medical's documentation structure and batch consistency have significantly simplified our QP release process for Thai-origin material.

Head of Quality

EU Pharmaceutical Importer

The structured onboarding process and transparent pricing model made it easy to build a business case internally. We went from qualification to first shipment in under 12 weeks.

Procurement Director

Licensed Distributor, Germany

Having dual-site production gave us confidence in supply continuity. The cultivar consistency across batches has been excellent for our formulation pipeline.

R&D Manager

Cannabis Manufacturer, Netherlands

Summarised feedback themes from B2B partners in qualification and supply. Named references may be available on request where confidentiality allows.

Three paths — choose yours

Whether you're an importer, manufacturer, or pharmacy, each inquiry captures exactly what the Verdant Medical team needs to qualify and respond within 48 hours.

For Importers

EU-licensed importers looking to establish or expand pharmaceutical cannabis supply from Thailand. MOQ discussion, documentation review, and logistics planning.

Importer Inquiry

For Manufacturers

Manufacturers evaluating GACP-documented dried flower for formulation and production. Sample requests, spec sheets, and batch capability review. (We do not supply extracts or concentrates.)

Request Samples

For Pharmacies

Dispensing pharmacies and pharmacy chains seeking documentation, compliance context, and supply qualification for medical cannabis products.

Pharmacy Inquiry