Who we are
VI.REL Pharma was founded in 1997 as a specialized consulting firm in the field of drug R&D.
Today, the VI.REL group consists of a team of international professionals with multidisciplinary experience, combining scientific, medical and regulatory knowledge.
VI.REL performs pharmacovigilance, regulatory intelligence, Module 1 and 2 registration dossier writing, document management in e-CTD format, and European-recognized medical writing activities.
Scientific Director, Principal Medical Writer, QPPV.
Regulatory Officer, Deputy QPPV.
Safety Officer, Quality Assurance.
Regulatory Affairs Assistant.
Pharmacovigilance Specialist and Deputy QPPV.