Cannabidiol Ph. Eur.

  • Cannabidiol Ph. Eur. 1
  • Cannabidiol Ph. Eur. 2
Product Description

Cannabidiol Ph. Eur. is a phyto-derived, highly purified cannabinoid active pharmaceutical ingredient isolated from Cannabis sativa L. and manufactured in accordance with the European Pharmacopoeia monograph for cannabidiol. After GMP release testing of the starting material, the product is purified and crystallised through validated process steps at our EU-GMP site in Schlattingen, Switzerland.

Appearance: white to off-white crystalline powder, no significant odour. Validated process; stability study ongoing (24 months). Not a controlled substance. DMF/ASMF under development.

Pack sizes: 100 g, 1 kg, 5 kg, 10 kg and 25 kg in stand-up bags according to the approved packaging specification. Storage at or below 25 °C, protected from light and tightly closed. 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
  • CAS Registry Number
    13956-29-1
  • Details
    Key specifications: CBD assay 98.0–102.0 %; total impurities ≤ 1.5 % (typically 0.3 %); THC ≤ 0.10 %; CBN ≤ 0.15 %; water ≤ 0.5 %; sulfated ash ≤ 0.1 %; residual solvents (Class III) ≤ 5000 ppm; pesticides according to Ph. Eur. / EC 396/2005 / FAO-WHO; heavy metals As ≤ 0.2 ppm, Cd ≤ 0.3 ppm, Pb ≤ 0.5 ppm, Hg ≤ 0.1 ppm; mycotoxins total aflatoxins ≤ 4 µg/kg, ochratoxin A ≤ 20 µg/kg; microbiology TAMC ≤ 200 CFU/g, TYMC ≤ 20 CFU/g, specified pathogens absent.

    Application areas: pharmaceutical development, formulation and use in finished medicinal products; compounding. Product type: phyto-derived pure cannabinoid API. Compliance: Ph. Eur. / GMP. CAS 13956-29-1.
  • 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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