Unpicking The Complexity Of Importer Of Record Processes In Globalized Clinical Supply Chains

A competent Importer of Record is a prerequisite to any successful global clinical trial. The role is vast and the remit wide, covering everything from ensuring imported goods comply with local law and regulations, payment of import duties, tariffs and fees; to risk mitigation and maximising opportunities to ensure the right drug, gets to the right patient at the right time.

Developing a robust distribution strategy for a globalised clinical trial is complex.  While there is no ‘one size fits all’ approach, Almac’s White Paper enables sponsors to better understanding the key elements of the role, the risks, the country-specific nuances and what general best practice looks like, so sponsors are better equipped to develop effective distribution strategies.