What do we do. We provide pharma regulatory, pharmacovigilance services. Including, regulatory submissions, coordination of procedures and processes, medical writings for generics products, package leaflet user testing for readability, EU e-CTD format dossiers publishing, artwork development, temporary assistance services etc. Who we are. Sveikuva is family owned regulatory/pharmacovigilance consulting company based in Lithuania. We are providing services to the companies in EU and CIS countries since 2003. Our experience. We gained experience with range of companies from big pharma companies to small marketing authorisation holders with few products. For big pharma we usually provide assistance services, for mid size pharma companies - local regulatory/pharmacovigilance manages with access to various internal computer systems services, while for small companies - we are fully assuring regulatory and/or pharmacovigilance activities.