Your study according to GLP? No problem!

Do you need GLP-compliant testing for your biocide registration or your medical device? Then please feel free to contact us. Dr. Brill + Partner has been certified as a GLP testing facility since June 2020 and registered with the BfR as a testing facility with the corresponding test category since July 2021.

This certification includes:

  • Tests for the determination of toxicological properties (category 2)
  • Tests for the determination of mutagenic properties (in vitro, in vivo) (category 3)
  • Microbiological and biochemical testing of cleaning, disinfection and sterilization processes) (category 9)

You don't know whether you should have a GLP test performed for your products? Please feel free to contact us! We will advise you comprehensively regarding the requirements for different legal areas (EU, USA/FDA), the demarcation to GMP and GCP and the possible laboratory tests.

What we can do for you:

Specifically, we have the following standards for you under GLP, which you are welcome to request at

  • ASTM E2755 (Bacteria-Eliminating Effectiveness of Healthcare Personnel Hand Rub)
  • AOAC 955.17 (Fungicidal Activity of Disinfectants)
  • EN 13697 (bactericidal and/or fungicidal activity of chemical disinfectants on non-porous surfaces without mechanics)
  • DIN EN ISO 10993-5 (tests for in vitro cytotoxicity of medical devices)

Is your standard/test standard not listed? Please contact us anyway, because we have further methods in the GLP pipeline.