JSC SVEIKUVA was established in 2003. Company 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. 

We operate in Central and Eastern European (CEE) countries, including Poland, Hungary, Bulgaria, Romania and Baltic States (Lithuania, Latvia and Estonia).

We have developed quality assurance system, which includes all our services. System is regularly audited by corporate Clients. Personal data management is GDPR compliant. 

Our aim

To work timely, reliably and advisedly, in order our clients could achieve their plans.

If You are looking for solution, advice us!

  • Professionalism.
    We are specialists in this field and like our activity, so we can guarantee the quality of our work.
  • Competitiveness.
    Individual solutions for a competitive price.
  • Confidentiality.
    We appreciate the cooperation, maintain confidentiality and seek for a long-term partnership