UAB SVEIKUVA was founded in 2003. Initially our activity was focused on regulatory affairs and translations services. Within next years our efforts and sustainable results had been recognized by company clients.
Since 2008 we started to provide full and local pharmacovigilance and package leaflets user testing for readability services. Shortly later offered eCTD dossiers publishing service.
Today UAB SVEIKUVA provides Regulatory Affairs and EU Regulatory Affairs project coordination services for medicines, medical devices, food supplements and cosmetics. Our activities covers from technical, pharmaceutical and medical writings to implementation and regional regulatory project coordination. UAB SVEIKUVA provides with local and regional pharmacovigilance support. Professional translation services of regulatory, pharmacovigilance and clinical trials documentation. We have established vendors network. Developed quality assurance with compliance monitoring and GDPR compliant personal data management system.
UAB SVEIKUVA is locally operating in following countries: Baltics (Estonia, Latvia and Lithuania), Bulgaria, Czech Republic, Hungary, Poland, Romania, Slovakia and in some other EU countries.
We value our clients and care about their aims. And we are proud, that for some of them we are serving almost since the very beginning of UAB Sveikuva establishment.
UAB SVEIKUVA developed quality assurance system which covers each of our service – regulatory affairs, pharmacovigilance and translations. We monitor our activities compliance and this pushes us for rapid adaptation to changing regulatory landscape and constantly improve our services.
Undoubtfully meeting the deadline is essential in our work. But it is not the only aim. There are another important targets to be met. We would like to invite you to contact us and hear our values and understanding of well done job.
UAB SVEIKUVA developed quality assurance system which covers each of our service – regulatory affairs, pharmacovigilance and translations. We monitor our activities compliance and this pushes us for rapid adaptation to changing regulatory landscape and constantly improve our services.
Undoubtfully meeting the deadline is essential in our work. But it is not the only aim. There are another important targets to be met. We would like to invite you to contact us and hear our values and understanding of well done job.