Backed up by medical support, several experts and key opinion leaders, our team can design for you:
Al monitoring services are provided by an experienced team of Clinical Research Associates. The monitoring of your study can take place in France and/or in other European countries.
Trial protocol Informed consent form CRF Patient diary
National Competent Authorities Ethics Commitee
Importation of products Storage in controled condition Delivery within 24/72 hours in Europe Return from investigator sites and destruction GDP, GMP ADR, IATA
Central Laboratory Biomarkers Bioanalysis Therapeutic drug monitoring Immunogenicity testing, genomic testing Ful range of services to support infectious disease drug development
Moreover we can perform a comprehensive menu of routine and customized safety and eficacy tests.
In the context of increasingly demanding regulations, we can assist you in the practice of pharmacovigilance, in whole or in part.
CRO services Flexible services for a tailored Trial