Pre-clinical and Clinical Trials

Capio Diagnostik a.s in Copenhagen is GLP certified, ISO 17025 accredited, GCP compliant and has been FDA audited.

The laboratory serves the pharmaceutical industry and the biotech industry with:

  • Method development
  • Method transfer
  • Method validation
  • PK-sample analyses
  • Bio-analytical Reports
  • Central laboratory services
  • Central logistics

Special strength in the following techniques:

  • ELISA
  • RIA
  • Molecular biology
  • Metal analyses

For further information please contact:

Yvonne Lech, Managing Director.:

Tel.:       +45 3374 3091
Mobile:   +45 2344 1284
Fax:       +45 3374 3030
E-mail:   yvonne.lech@capio.dk