• We are highly specialized in implementation of clinical trials and drug regulatory affairs in Slovenia, Croatia, Serbia, Bosnia & Herzegovina and Macedonia
• We have local expertise - we understand all of the regulatory, medical, and cultural issues in the countries where the trial is taking place because we are native of the countries in which we are operating
• We are native speakers but also fluent in English
• We are up to date with the national laws and requests from Regulatory agencies and Ethics Committees
• Our excellent reputation with Regulatory authorities in the region enables us to reach Regulatory Approvals in timely manner and fast start up of the projects
• We are up-to-date with the social and political situation of the society, thus understanding status and current climate in everyday life of investigators and patient population in their country
• We have strategic partnership with physicians from private practice, academic health centers and governmental hospitals
• We are a team of 40 professionals trained and certified in ICH/GCP requirements and following  FDA and EMEA standards
• We are flexible company with very short reaction time in starting and performing projects
• We offer the service of official representation on behalf of the sponsors towards European agencies and  Ethics Committees

  We are smart, hard working team with lots of experience!

• Why choose SEE
• Why choose SEA

 

 

 

 

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