Preclinical research in Germany
Germany has a broad base of preclinical labs, from specialist in vitro and safety pharmacology groups to full-service toxicology facilities, and serves both European and international sponsors.
Animal research follows EU Directive 2010/63/EU as implemented in German animal welfare law, and GLP compliance is monitored by regional authorities under the OECD Mutual Acceptance of Data system, so studies run in Germany can support submissions in the US and other member countries.
Preclinical CROs in Germany
Showing 1 CRO with a site in Germany. Order rotates daily so no lab is permanently listed first.
Questions to ask a CRO in Germany
- Will the study run at the site in Germany, 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.