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1T06P / 1T07W- 1T3FJ


S. aureus + P. aeruginosa + E. coli + C. albicans + Validation (to avoid false negative)


Tests are designed primarily to determine whether a product complies with SCCS and ISO 17516 or EP/BP <2.6.12><2.6.13><5.1.4> specification for microbiological quality


2 weeks for Pathogens + report: 4 weeks, 3-5 weeks for validation + report: 6 weeks. Validation must be done before


Optimal: 100 g

Minimal: 10 g per test


ISO 22718, ISO 22717, ISO 21150 and ISO 18416

Or USP <62>

Or European Pharmacopeia <2.6.13>


The potential inhibition of microbial growth must be neutralized in order to allow detection of viable microorganisms.

This test relies on detecting and identifying characteristic colonies on selective agar.


GMP (Good Manufacturing Practice) for cosmetics - ISO 22716

Production laboratory

  • Eurofins Pharma Quality Control (ACE), Les Ulis, FRANCE
  • Eurofins BioPharma Product Testing, Milan, ITALY
  • Eurofins BioPharma Product Testing Hamburg GmbH, Hamburg, GERMANY
  • Eurofins BioPharma Product Testing Munich GmbH, Planegg, GERMANY
  • Eurofins Product Testing, Cosmetics & Personal Care Spain
  • Eurofins Lancaster Laboratories, Dungarvan, IRELAND
  • Eurofins Polska, Malbork, POLAND
  • Eurofins Bel/Novamann s.r.o., Nové Zámky, SLOVAK REPUBLIC
  • Eurofins Bactimm, Nijmegen, THE NETHERLANDS
  • Eurofins Exova, Camberley & Edinburgh, UK
  • Eurofins AMS Laboratories, Sydney, AUSTRALIA
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