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SVEIKUVA was established in 2003. It is providing pharma industry with regulatory affairs consulting services through product lifecycle (from pharmaceutical and medical writings until obtaining and maintaining marketing authorisations in local level), pharmacovigilance and translations/ localisations services. Sveikuva operates in Central and Eastern European (CEE) countries, including Poland, Hungary, Bulgaria, Romania and Baltic States (Lithuania, Latvia and Estonia). The company has developed quality assurance system, which includes all our services. System is regularly audited by corporate Clients. Personal data management is GDPR compliant.



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