Standardized Cannabis Extract Type II

  • Standardized Cannabis Extract Type II 1
  • Standardized Cannabis Extract Type II 2
Product Description

Standardized Cannabis Extract Type II is prepared from validated Cannabis Distillate (THC) and Cannabis Distillate (CBD) and adjusted with medium-chain triglycerides (MCT) to the required cannabinoid profile. The use of refined distillates provides a cleaner and more defined matrix and supports reproducible formulation performance. The result is a transparent yellow-golden liquid for compounding, pharmaceutical development and bulk medicinal-product applications.

Appearance: yellow-golden, transparent liquid. Current release specification available; stability study pending. Controlled-substance status depends on the cannabinoid ratio and the destination market.

Pack sizes: 100 g, 250 g and 1 kg according to the approved packaging specification. Storage at or below 25 °C, protected from light. Detailed specification, example CoA and safety data sheet on request.

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Canexis Pharma AG

  • Country/Region:
    Switzerland
  • Founded:
    2020
  • On CPHI since:
    2025
  • Certificates:
    3
  • Employees:
    1 - 24
Company types
CMO/CDMO
Generics/Biosimilars Manufacturer
Manufacturer/Innovator
Pharmaceutical company
Primary activities
API Producer
Custom Manufacturing/Custom Synthesis
Generic APIs producer
Intermediates Manufacturer
Natural Extracts
View company profile
Categories
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Specifications
  • Details
    Key specifications: cannabinoid setting THC 0–25 % and CBD 0–25 % according to the agreed product setting; CBN ≤ 2.5 %; water ≤ 0.5 %; residual solvents (Class III) ≤ 2500 ppm; pesticides according to Ph. Eur. / EC 396/2005 / FAO-WHO; heavy metals As ≤ 2.0 ppm, Cd ≤ 1.0 ppm, Pb ≤ 5.0 ppm, Hg ≤ 0.1 ppm; mycotoxins aflatoxin B1 ≤ 2 µg/kg, ochratoxin A ≤ 20 µg/kg; microbiology TAMC ≤ 2000 CFU/g, TYMC ≤ 200 CFU/g, specified pathogens absent.

    Application areas: compounding, bulk medicinal products, pharmaceutical development. Product type: standardized cannabinoid bulk product / API / bulk finished medicinal product, MCT-based adjusted cannabinoid matrix (distillate-based). Compliance: GMP / API / bulk medicinal product. Multi-component botanical preparation, no single CAS number.
  • Selling Points
    International Approvals/Standards; Natural Ingredients; Place of Origin; Prompt Delivery; Quality Service; Small Orders Accepted; Manufactured in Switzerland under EU-GMP Part I and Part II licences, a Swissmedic manufacturing licence and a Swiss narcotics licence. Starting material from around ten qualified cultivation partners working to WHO-GACP, released under GMP against Ph. Eur.-based specifications. Release testing by qualified external GMP laboratories; Certificate of Analysis with every shipment. Technical/quality agreements, on-site audits, national regulatory documentation and DMF/ASMF support available. Shipping worldwide from Zurich Airport with temperature monitoring. Samples and technical batches on request.
  • Supplied from
    Switzerland
  • Measured In
    gram; kilogram
More specifications Fewer specifications
Sales Markets
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Canexis Pharma AG

  • Country/Region:
    Switzerland
  • Founded:
    2020
  • On CPHI since:
    2025
  • Certificates:
    3
  • Employees:
    1 - 24
Company types
CMO/CDMO
Generics/Biosimilars Manufacturer
Manufacturer/Innovator
Pharmaceutical company
Primary activities
API Producer
Custom Manufacturing/Custom Synthesis
Generic APIs producer
Intermediates Manufacturer
Natural Extracts
View company profile

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