Let's prove it.

Why Vizera?

We are fully aware that the applicability of the clinical trial results is of utmost importance. Thus, we are specifically focused on the preparation of the study protocol – the careful setting of study objectives, ensuring an appropriate sample size and minimising clinical trial biases. Only then can the product’s effectiveness be accurately evaluated and reliable results obtained.


Make use of our competitive advantages:

  • Full service CRO 
  • Multidisciplinary team who understands medical devices and nutraceuticals market needs
  • Trials are completed within budget and on time
  • Very competitive pricing
  • Highly professional and motivated network of investigators
  • Highly skilled and well-trained staff
  • Clinical sites in the Balkan region, most of them located in Slovenia, Croatia and Serbia
  • Clinical trials designed in accordance with MEDDEV 2.7/4, EN ISO 14155-1:2011, GCP and other relevant guidelines and legislation
  • Full support for obtaining the CE mark for medical devices
  • Full support for health claim or novel food application