• Hessenring 15i, Mörfelden-Walldorf, Hessen 64546 View on Map
  • Telephone: 069 / 2475 778 40
  • Social Links:


  • Sectors Pharmazie
  • Posted Jobs 3
  • Viewed 465
  • Founded Since 1850
  • Website Http://www.cansativa.de

Company Description

Professionalizing Medical Cannabis.

Founded in 2017, Cansativa is a GMP-certified pharmaceutical company and holds a GDP pharmaceutical wholesale license to trade in controlled substances. From its headquarter in Moerfelden-Walldorf, Germany, Cansativa and its subsidiaries work to professionalize the medical cannabis market, eliminate stigmatization and to permanently reduce prices for patients. As an owner-managed company, our growth target is linked to a long-term vision – we want to set industry-wide benchmarks.

Since the very beginning, Cansativa has operated its own distribution and fulfillment center, and as one of its industry’s “first movers”, it has become one of the largest independent manufacturers, importers, and distributors of medical cannabis in Germany. From its location in Mörfelden-Walldorf, the company supplies pharmacies and pharmaceutical wholesalers throughout Germany. Cansativa is uniquely positioned as „one-stop shop“ with a comprehensive multi-brand portfolio in the German market and secures the supply of urgently needed medical cannabis pharmaceuticals. Cansativa is the only company that has been contracted by the Federal Institute for Drugs and Medical Devices (BfArM) to distribute and to provide logistics and wholesale services for the entire German cannabis production for the next four years. Through our top-notch partnership network with well-known supplier, pharmacists can order a broad range of products such as API, pharmaceuticals and medical devices via our Cansativa platform.

Cansativa also offers pharmaceutical companies a platform for market access. We have developed into a full-service provider for the medical cannabis market. Cansativa is a service provider for all aspects of medical cannabis sales: we assist in communicating with authorities, certification processes, project and process management and all matters in the area of regulatory affairs.