ICON interview: Insights on the new EMA guidelines for computerised systems and electronic data in clinical trials
OSP spoke to Vesta Marciulioniene, director global regulatory clinical services at ICON Biotech, a contract research organisation who shares insights on the new EMA guideline for computerised systems and electronic data in clinical trials and what new expectations it sets for the clinical research industry.
Vesta Marciulioniene European Union Global Regulatory Clinical Services European Medicines Agency Computerised Systems Electronic Data
Source: outsourcing-pharma.com