News

LAUS has always paid particular attention to sustainability by offering technical solutions to improve and optimize the efficiency of processing and analysis cycles. We contribute to global sustainability efforts not only by minimizing the consumption of water and of energy, but also by reducing the use of natural resources. E.g. we reuse packaging material from the large number of sample shipments we receive. #LAUSGmbH #sustainability #reuse #recycle

Do you have a hazardous mixture for consumer or professional use and need to generate a UFI (Unique Formula Identifier) and comply with the new PNC requirements (Poison Notification Centre)?

Substances from three different areas may require Endocrine Disruptor Assessment:
- Chemicals under REACH
- Biocidal Product
- Plant Protection Products
LAUS can support you with ecotoxicological studies for your Endocrine Disruptor Assessment.
Contact us for more information and a price quotation.
https://www.laus.group/en/services/endocrine-properties

In order to fight the current Covid-19 pandemic effectively fast-tracking the availability of disinfectants is possible.
A cross-industry alliance has published a practical guide to assist companies to understand and comply with obligations of biocides legislation during and after the pandemic.
Please, click here for more information.

Um die derzeitige Covid-19-Pandemie wirksam zu bekämpfen, ist es möglich, ist ein beschleunigtes Verfahren möglich, um die schnelle Verfügbarkeit von Desinfektionsmitteln zu ermöglichen. Eine branchenübergreifende Allianz hat einen praktischen Leitfaden veröffentlicht, der Unternehmen dabei hilft, die Verpflichtungen der BPR während und nach der Pandemie zu verstehen und einzuhalten. Bitte klicken Sie hier für weitere Informationen.

The Effective Date of the new MDR (EU) 2017/745 has been postponed by the European Parliament on 17 April 2020. This means the new MDR will come into force on the 26^th of May 2021.

All biocidal products must be authorised before being placed on the market and the active substances contained in the biocidal products must have been approved in advance (BPR (EU) No 528/2012).

Has the dossier evaluation by ECHA revealed that the data situation is "irrelevant, not reliable (Klimisch Code 3 or 4) or not sufficient"?
And do you need to present new or supplementary data?