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Smooth Drug Development, CLINICAL TRIALS IN THE CIS, EASTERN EUROPE, AND CENTRAL EUROPE

CLINICAL TRIALS IN THE CIS, EASTERN EUROPE, AND CENTRAL EUROPE

Smooth Drug Development, PHASE I STUDIES

PHASE I STUDIES

Smooth Drug Development, ISO 9001 certified

ISO 9001 certified

Smooth Drug Development, BIOEQUIVALENCE TRIALS

BIOEQUIVALENCE TRIALS

Smooth Drug Development, POST-REGISTRATION STUDIES

POST-REGISTRATION STUDIES

Smooth Drug Development, ISO 22301 certified

ISO 22301 certified

Smooth Drug Development, GDRP compliant

GDRP compliant

Smooth Drug Development

Full-service CRO that provides support to pharmaceutical and biotechnology companies in 

drug development from concept to post-marketing surveillance. To learn more →

 
 
 
 
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About us

Smooth Drug Development is a full-service Contract Research Organization (CRO), conducts clinical trials in Russia, CIS and Baltic States

We provide a full range of clinical services for the pharmaceutical and biotech industry including management of phase I-IV clinical trials and bioequivalence studies. Smooth Drug Development is known within the industry for its experience in managing clinical trials, successful clinical oversight, quick and stable patient enrollment and retention, and for providing robust solutions to Sponsors. Our team will make sure that your clinical study is completed on time, within budget, and with the highest quality of data. We always aim to exceed expectations of our Clients.