Smartpharm

best solution for you

We are your partner of choice for pharmaceutical market access in the southeastern Europe and CIS regions.

covering the complete product life-cycle

We can take care of your product registration, clinical studies, market positioning, promotion materials, and sales.

lean and effective

Thanks to our lean organisational structure, we can make and implement decisions quickly.

international experience, local knowledge

Our team has worldwide experience in the pharmaceutical industry as well as in-depth knowledge of local culture and customs.

top quality service

We have experts on our team for all fields covered and work hand-in-hand with the best solution providers in each region.


Clinical trials

Clinical trials are conducted to asses effectiveness and safety of new or already marketed drugs. Their results are an essential part of regulatory dossiers and marketing strategies. In some countries in SEE and CIS regions, local clinical trials are advisable or even compulsory.

Ability to support our product portfolio with in-house know-how about clinical trials is of strategic importance for Smartpharm. We can provide or assist in:

  • clinical trial design and project development
  • preparation of study documentation
  • data management
  • statistical analysis
  • final report writing
  • planning, preparing and submitting publications

Through our in-house expertise for design and support of clinical trials, we are providing support for all important components in Phase III and Phase IV of clinical trials.