Support safety management throughout product lifecycle.
SFL’s Pharmacovigilance team has long-standing experience in EU and Swiss pharmacovigilance processes and supports headquarter companies and their affiliates in achieving pharmacovigilance excellence in compliance with good pharmacovigilance practice (GVP) regulations. SFL team members can act as EU Qualified Person Pharmacovigilance (QPPV) and local QPPV, conduct gap analyses and PV audits, and set-up PV Quality Systems and Pharmacovigilance System Master Files (PSMF).
