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IN PARTNERSHIP


clinical trials globally increases supply chain efficiencies and reduces drug costs. As the number of clinical trials in emerging markets increases, the demand for reference drugs, or comparators, is mounting.


T


The US and Europe are the biggest clinical trial markets in the world, and the fierce competition between drug manufacturers to get their products to market first is intensifying. Clinical trial sponsors are therefore turning to emerging markets to source comparators efficiently and cost-effectively. Increased demand puts comparator sourcing professionals under immense pressure to source enough quantities of comparator products within the right time frames and budget restrictions. At Clinical Services International (CSI), as a


he prevalence of clinical trials in emerging markets is soaring. With the right infrastructure in place, conducting


leading global comparator sourcing partner, we understand the benefits and risks involved in comparator sourcing in emerging markets for global clinical trials.


Comparator studies Comparator studies aim to prove the efficacy of new or investigational drugs compared to the existing standard of care, also known as the comparator. To ensure treatments are effective before seeking approval and going to market, it is necessary to securely source comparators including reference-listed drugs (RLD) and non-investigational medicinal products (NIMPs) on a global scale.


Pharmaceutical companies and contract research organisations (CROs) must have robust comparator sourcing strategies in place to ensure that comparator drugs are supplied to clinical trial sites without disruption. Working


16 | Clinical Trial Supply Handbook


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