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LifeScientis Consulting core activities lie in global toxicology with specific expertise in Endocrine Disruption and Nanotechnology Safety assessment. 

We work as an Open company with a broad network of experts enabling us to address risk assessment for all Life Sciences sector's stakeholders.

A dedicated expert assists you with advisory actions, support, training, data support & interpretation, assistance to conception and optimization of your existing non-clinal programs.



Operational services

We conduct the toxicological risk assessment of your compound with high-quality scientific interpretation

Non-Clinical / Preclinical Drug Safety • IND Enabling Studies • Study Design, Placement & Monitoring • Data Analyses • Report Writing and/or Review • Integrated Summary Document Preparation • Clinical Investigator Brochures • Toxicology Portions of Regulatory Submissions  

Project Management Support

We assist your team in non-clinical toxicological project management

Non-Clinical Drug Development Strategies • Development Team Involvement / Leadership • Project Management • CRO Selection • Expert Report / White Paper Preparation • Manuscript Preparation • Scientific Literature Reviews • Due-diligence Reviews • Academic Liaison



Our guidelines help you to

establish a safety strategy in your R&D programs

anticipate regulatory changes to come

ensure the safety of use of your molecules & devices