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22.02.2018

LAUS is expanding

LAUS is expanding

We need more room to realize our vision for the future. Since the company has been steadily growing in the past years, we will expand from 1.500 m2 to 2.000 m2.

On Feb. 21st 2018 we had our ground-breaking.

Come and follow this exciting development:

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05.10.2017

All three in vitro skin sensitisation studies available under GLP

LAUS NEWS: All three in vitro skin sensitisation studies available under GLP

LAUS has established and fully validated the h-CLAT (human Cell Line Activation Test, OECD 442E) and is now able to perform all three studies available for in vitro skin sensitisation testing under GLP conditions (h-CLAT, DPRA, LuSens).

The h-CLAT (human Cell Line Activation Test) uses the human monocytic leukemia cell line THP-1. The up-regulation of the surface molecules CD54 and CD86 as markers of dendritic cell activation is measured by flow cytometry following cell staining with fluorochrome-tagged antibodies.

In vitro skin sensitisation testing can substitute the corresponding in vivo study, the LLNA (OECD 442B and 429), in many cases. Unlike the LLNA, which is a stand-alone study, in vitro skin sensitisation testing consists of an array of three studies, each of them targeting a key event in the Adverse Outcome Pathway (AOP) of skin sensitisation. A substance can be rated as a sensitiser with two consistent positive results.

     

Key event of AOP

 

Study

OECD

1

covalent interaction with skin proteins

DPRA

442C

2

keratinocyte response

LuSens

based on 442D

3

dendritic cell activation

h-CLAT

442E


The tests are interesting for clients from the following regulatory areas:

  • REACH (EC 1907/2006)
  • The CLP Regulation (EC 1272/2008)
  • The Biocidal Products Regulation (EC 528/2012)
  • The Plant Protection Products Regulation (EC 1107/2009)
  • The Cosmetics Regulation (EC 1223/2009)
  • And screening at non-regulatory stages of product development

 

Want to know more? Contact us at info@laus.group or http://www.laus.group

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