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 Scientificservice@brillhygiene.com:

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.