Lumis International GmbH

About Lumis International GmbH

Lumis International GmbH - Your partner in clinical efficacy For Drug development companies not located in the European Union Lumis offers to act as their legal representative according to the EU Clinical Trial Directive 2001/20/EC Art. 19 (1) and the Clinical Trial Regulation 536/2014 Art. 74 (1) Especially small to midsize companies have to outsource the majority of activities to perform their clinical trials. Lumis has developed tools to define the best • Outsourcing Strategy and Vendor Selection process • Vendor management approach • Risk based Clinical Trial Oversight Management tools Get your clinical operations inspection ready and your clinical trials due diligence compliant! For more information, visit our website or contact us at info@lumisinternational.com.