Laura Ardigó, MD - Clinical Research Consultancy

I offer expert clinical research consultancy services in Latin America for Sponsors, CROs and research sites to help them accomplish with confidence regulatory compliance, research ethics, subject protection and quality data for their clinical trials in the region. We provide training, can assist in site/ CRO/ vendor selection, perform close monitoring of projects and vendors, audit sites, CROs and vendors, develop and improve research sites (old or new) and write and implement SOPs. We can also train and coach new research staff at sites and companies or cover specific roles within clinical trials (monitor, medical monitor, project management, etc)