Providing compliance for your clinical trials

Quality and Authorisations

Nomeco CTSM combines profound quality insight with highly experienced staff in clinical trials in order to provide the best solutions for our clients throughout the supply chain for the clinical trials. Nomeco CTSM is audited 10-12 times per year by existing and new clients and with the solid and standardised processes, we are at all times audit ready.      

Nomeco is fully authorised by Danish Medicines Agency to import, manufacture and distribute pharmaceuticals, controlled drugs and clinical trial products. Furthermore, Nomeco is certified according to ISO 9001 standard. These are the foundation for our high quality standard ensuring study conduct compliant to GDP, GMP and GCP regulations.

Please find our authorisations here

  • GDP license: Authorisation for wholesale distribution of pharmaceuticals

  • GMP license: Manufacturing and Importation Authorisation

  • ISO certificate: ISO 9001 certificate


Your Benefits

  • Balancing IMP AVAILABILITY and minimising product waste
  • Reducing cost by MINIMAL WASTE of IMP
  • STREAMLINED and optimised supply chain


Nomeco CTSM
Borgm. Christiansens Gade 40
DK 1790 Copenhagen V