Porsolt has 30 years of experience providing services in safety pharmacology. Our Scientists develop, validate and perform studies in fully compliance with the principles of Good Laboratory Pratices.

Porsolt team works to meet your needs in every phase of the discovery and the preclinical development of your compound.
Our GLP expertise includes:

> Protocols / study Reports
> SOPs
> Critical phases inspection (in study)
> Computerized system
> Scientific equipment qualification
> Chemistry method transfer or development
> Assay validation
> Sample analysis
> Stability assay
> Drug management and storage
> Samples management and storage
> Data management
> Archiving