Preclinical CROs in Denmark

5 contract research organizations in our directory list a site in Denmark. 1 reports GLP capability and 0 report AAALAC accreditation. Compare services, species and accreditations below, and contact labs directly from their profiles.

5 CROs 1 GLP

Preclinical research in Denmark

Among the CROs listed in Denmark, the most common services are In Vivo Efficacy, Pharmacokinetics, Oncology Models and MRI Studies. The species they most often work with are Mouse, Rat and Rabbit.

Showing 5 CROs with a site in Denmark. Order rotates daily so no lab is permanently listed first.

Gubra

Horsholm

Danish preclinical CRO and peptide discovery company known for metabolic, liver and kidney disease models with AI-supported histology and 3D imaging readouts.

Hepatic Disease Models Histopathology In Vivo Efficacy Metabolic Disease Models Renal Disease Models Mouse Rat

Scantox

Lille Skensved GLP

GLP-accredited preclinical CRO headquartered in Denmark with sites in Sweden, Austria and the UK. Known for Gottingen minipig work and regulatory toxicology, with discovery pharmacology including CNS and…

CNS Disease Models Dermal Toxicity Formulation Development Genetic Toxicology GLP Toxicology Minipig Mouse Rabbit Rat

Bioneer

Horsholm

Danish non-profit research CRO offering customised cell models, assays and translational research services.

Biomarker Analysis In Vitro Pharmacology Method Development

Biotest Facility

DK

Independent Danish CRO focused on early in vivo pharmacology in rodents, with particular expertise in mouse cancer and immuno-oncology models.

In Vivo Efficacy Oncology Models Pharmacokinetics Syngeneic Models Mouse Rat

Minerva Imaging

Olstykke

Danish preclinical imaging CRO offering PET, SPECT, CT and MRI studies, radiopharmaceutical development support and oncology efficacy models.

CT Imaging In Vivo Imaging MRI Studies Oncology Models PET Imaging Mouse Rat

Questions to ask a CRO in Denmark

  • Will the study run at the site in Denmark, or could work be moved to another of your facilities?
  • How do you receive test article shipments, and what import permits or customs paperwork do you handle?
  • Can our team visit the facility before the study starts and during critical phases?
  • Which regulators and GLP monitoring authorities have inspected this site, and when?
  • What is your current lead time for our species at this site?

For a full checklist, see our CRO selection guide.