Regpharm Clin

CRO · Spain

As a Regulatory Affairs consultant, I offer expert assistance to clients with all regulatory aspects related to the submission of clinical studies, from Phase I through Phase III (Pivotal), as well as Non-Interventional studies and management of the CT from study start up through close-out of the study globally (Feasibility, Site Selection, Site Identification, Clinical Operations Management (CRA, CPM, BioStatisticals, Data Management, GCP Audits..etc). Source (opens in a new tab)

Website: https://regpharmaclin.com/
Headquarters: ES
Provider types: CRO, clinical CRO