Sveikuva provides regulatory affairs services for medicines, medical devices, food supplements and cosmetics since 2004. Scope of our regulatory activities covers early product lifecycle steps and includes services from technical, pharmaceutical and medical writings to global regulatory project coordination. Sveikuva has developed quality assurance system, including standardised working procedures and processes, which allows to assure compliance of regulatory affairs services.
Work organisation gives possibility to provide client with clear and convenient contact point, assure fast submission of procedures and involved back-ups.
We are locally operating in Baltics (Estonia, Latvia and Lithuania) and following countries:, Bulgaria, Czech Republic, Hungary, Poland, Romania, Slovakia and in some other EU countries.
We provide the following services:
Additional services:
Sveikuva provides regulatory affairs services for medicines, medical devices, food supplements and cosmetics since 2004. Scope of our regulatory activities covers early product lifecycle steps and includes services from technical, pharmaceutical and medical writings to global regulatory project coordination. Sveikuva has developed quality assurance system, including standardised working procedures and processes, which allows to assure compliance of regulatory affairs services.
Work organisation gives possibility to provide client with clear and convenient contact point, assure fast submission of procedures and involved back-ups.
We are locally operating in Baltics (Estonia, Latvia and Lithuania) and following countries:, Bulgaria, Czech Republic, Hungary, Poland, Romania, Slovakia and in some other EU countries.
We provide the following services:
Additional services: