Biocides
Support and high quality advice
In compliance with GLP standards and new legislation for biocidal products, Eurofins' pharma services provides you services to support you in fulfilling regulatory requirements for active substances and formulations registration.
Complete and competitive analysis offer
Eurofins' pharma services is GLP accredited by Italian Health Authorities to perform chemical, toxicological and efficacy studies on active substances and formulations with a disinfectant or antimicrobial activity (disinfectants for environments, for skin of surface antimicrobial).
The GLP accreditation includes also eco-toxicity and biodegradability test on chemicals, both active and inactive substances.
Eurofins' pharma services approach is to develop a study group with a very wide range of skills, capable to satisfy customer requirements on new biocidal substances and/or preparations to be placed into the EU market from the R&D stage to the 'go in the market' stage.
Both standard and customized analysis by adapting common standard protocols (always under GLP accreditation) can be performed, together with a wide range of analysis useful to produce a biocidal substance or product, according with 528/2012 EU Regulation requirements and its following updates.
A deep competence has been exploited in virucidal efficacy studies, covering both standard testing to cover regulatory requirements and ad-hoc designed protocols to objectivate specific claims or to support R&D stage in new products development.
The following tests, according GLP requirements, following OECD, CEN, ISO, ICH and ASTM harmonized methods, are performed:
- Efficacy studies
- Eco-toxicological and biodegradability studies
- Chemical and stability studies
- Virucidal activity and virucidal inactivation studies
For further information please contact us: pharma@eurofins.com