Your Pharmaceutical Cannabis Supply Partner
Structured offtake agreements for licensed European pharmaceutical distributors
Highveld Farms is being established as a dedicated B2B pharmaceutical cultivation operation, structured to supply pharmaceutical-grade dried cannabis flower to licensed European distributors, importers, and pharmaceutical companies. We will not sell to the public or operate dispensaries. Our sole focus is supplying licensed European pharmaceutical distributors.
How Partnership Works
A structured pathway from first contact to ongoing supply
Engage
Initial Consultation
We begin with a thorough consultation to understand your volume requirements, chemovar preferences, quality specifications, and market-specific regulatory needs.
- Volume and format requirements
- Chemovar profile preferences
- Regulatory and import documentation needs
- Delivery cadence and logistics planning
Qualify
Due Diligence & Evaluation
Mutual due diligence ensures alignment on quality standards. We provide samples for independent evaluation and negotiate quality agreements tailored to your market.
- Mutual due diligence and credential verification
- Sample provision and independent lab evaluation
- Quality agreement negotiation
- Pricing and offtake term structuring
Supply
Ongoing Production & Delivery
Production to your agreed specifications with batch-by-batch Certificate of Analysis documentation, coordinated logistics, and dedicated account management.
- Production to agreed specifications
- Batch-by-batch CoA documentation
- Coordinated export logistics
- Dedicated account management
Partnership Credentials
Designing Europe's most reliable pharmaceutical cannabis supply chain
European Distribution Targets
Structured for partnerships with licensed pharmaceutical distributors across the UK, Germany, and EU markets. Offtake discussions active with distributors holding required import authorisations.
EU-GMP Certified Importers
Target distribution partners maintain EU-GMP certified receiving and storage facilities, ensuring pharmaceutical-grade handling from greenhouse to European pharmacies.
Multi-Market Reach
Through a planned network of licensed partners, HVF is targeting key European pharmaceutical markets including Germany, France, Poland, and the United Kingdom.
Partner Testimonials — Coming Soon
Named partner logos and testimonial quotes will be added to this section with explicit written approval from each distribution partner.
Target Markets
Pharmaceutical cannabis market access across Europe
Through targeted partnerships with licensed pharmaceutical distributors, Highveld Farms will access key European medical cannabis markets. Each market has distinct regulatory requirements — our compliance architecture is designed to meet them all.
Germany
Regulator: BfArMMarket Context
Europe's largest medical cannabis market with established import frameworks and growing patient demand. Legal prescriptions available across all therapeutic areas.
Access Pathway
EU-GMP certified product imported through licensed pharmaceutical wholesalers under BfArM authorisation. GACP documentation required for cultivation-origin compliance.
France
Regulator: ANSMMarket Context
Expanding medical cannabis framework with a generalized access programme. Growing demand for pharmaceutical-grade imported flower from compliant origins.
Access Pathway
Product imported under ANSM oversight through licensed pharmaceutical distributors. Full EU-GMP and GACP documentation chain required for market authorisation.
Poland
Regulator: GIFMarket Context
A rapidly emerging medical cannabis market in Central Europe with increasing physician awareness and patient access through pharmacy prescriptions.
Access Pathway
Pharmaceutical imports facilitated through licensed importers under Chief Pharmaceutical Inspector (GIF) oversight. EU-GMP compliance is the baseline requirement.
United Kingdom
Regulator: MHRAMarket Context
Specialist-prescribed medical cannabis market operating under MHRA oversight. Growing acceptance within private clinics and NHS pilot programmes.
Access Pathway
Product imported through MHRA-licensed importers holding appropriate controlled drug licences. Mutual recognition of South African SAHPRA documentation supports compliance pathway.
Export & Logistics
Supply chain designed from Potchefstroom to European pharmacies
Harvest to European Warehouse
14
Days
Targeted timeline from final quality release to receipt at distribution partner’s EU-GMP certified European facility
Supply Chain Flow
Six stages from cultivation to patient
Cultivation & Harvest
Potchefstroom, South Africa
Pharmaceutical-grade cultivation designed under GACP-compliant protocols in a sealed Venlo greenhouse.
Quality Assurance & Release
On-Site Laboratory
Full analytical testing suite — potency (HPLC), terpene profiling (GC), microbial screening, heavy metals, pesticide residue, and mycotoxin analysis.
Pharmaceutical Packaging
On-Site Packaging Facility
EU-import compliant packaging with tamper-evident seals, batch labelling, and full documentation including Certificate of Analysis.
Air Freight Export
OR Tambo International Airport
SAHPRA-permitted export via temperature-controlled air freight from Johannesburg to European hub airports.
EU-GMP Receiving Facility
European Distribution Hub
Targeted receipt at partner's EU-GMP certified facility for incoming quality verification, storage, and market-specific repackaging where required.
Pharmacy Distribution
European Markets
Targeted distribution to pharmacies and healthcare providers through licensed pharmaceutical supply chains in Germany, France, Poland, and the UK.
Export Documentation
Every shipment will be accompanied by comprehensive pharmaceutical documentation ensuring full traceability from cultivation through to patient.
Certificate of Analysis
Batch-specific analytical results from accredited laboratory
SAHPRA Export Permit
Section 22C export authorisation for each shipment
Import Country Permit
Destination-specific import licence documentation
Batch Records
Complete cultivation, processing, and packaging records
GACP Compliance Certificate
Good Agricultural and Collection Practices documentation
Cold Chain Records
Temperature logging throughout transport and storage
Cold Chain Integrity
Temperature-controlled logistics will be maintained throughout the supply chain. Continuous data logging devices will accompany every shipment, providing verifiable proof of storage conditions from facility to receiving warehouse. Any excursion will trigger immediate investigation under our CAPA framework.