2014
DOI: 10.2478/sjph-2014-0011
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Current regulatory and market environment for biosimilars in Serbia

Abstract: Background: Biosimilars are currently a reality of the pharmaceutical market in the European Union. This paper describes the current regulatory policy for approving biosimilars both in the European Union and in

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“…The proportion of total costs attributed to anti-cancer treatment in recurrent MM was 92% for lenalidomide-based regimens, 90% for bortezomibbased regimens and 54% for thalidomide-based protocols. The higher proportions of drug costs in comparison to other studies [39,40) can be explained by the fact that the pricing of medications in Serbia is based on the European Union recommendations [42], while the unit costs of diagnostic procedures and inpatient care are significantly lower in Eastern Europe.…”
Section: Discussionmentioning
confidence: 75%
“…The proportion of total costs attributed to anti-cancer treatment in recurrent MM was 92% for lenalidomide-based regimens, 90% for bortezomibbased regimens and 54% for thalidomide-based protocols. The higher proportions of drug costs in comparison to other studies [39,40) can be explained by the fact that the pricing of medications in Serbia is based on the European Union recommendations [42], while the unit costs of diagnostic procedures and inpatient care are significantly lower in Eastern Europe.…”
Section: Discussionmentioning
confidence: 75%