A CRO with over 20 years’ experience, compliant with standards (ICH, CDISC, etc.) and regulatory requirements (ANSM, EMA, FDA…).
Working with life sciences stakeholders, we design, set-up, and coordinate studies throughout Europe thanks to our network, from the writing of protocols to the publication of scientific articles.
PHARMA LABS – BIO/MEDTECHs – MD/IVD – COSMETICS – NUTRITION – VETERINARY
Phase II to IV studies
Transversal or longitudinal studies
Cohort studies, registries
Observatories, Post-MA studies
Determine the dose-response relationship and dosage to be used during a subsequent study phase for comparing the drug to placebo.
Set up and lead a prospective, multicenter phase IV clinical trial.
Set up and lead a PMCF (post marketing clinical follow-up) and patient recurrence evaluation study.
Develop and apply a statistical (propensity score) and medical analysis method for a non-randomized study.
Develop a clinical evaluation strategy for the CE marking of an image-processing algorithm.
Develop and demonstrate the reliability of an automated measurement system for a diagnostic evaluation test for a disease.
Soladis Clinical Studies - France
Les Paraboles IIa
84 boulevard du Général Leclerc
59100 Roubaix - FRANCE
Soladis - France (HQ)
6-8 rue Bellecombe
69006 LYON - FRANCE
Soladis GmbH - Switzerland
Lange Gasse 15
Soladis Inc. - USA
185 Alewife Brook Pkwy, Unit 210
Cambridge, MA 02138-1100