OverviewNowadays the majority of Clinical Trials are multi-national involving various countries, so the main (“master”, typically English) versions of Study Materials should be adapted as per country-specific requirements in order…

OverviewAs per Good Clinical Practice (GCP) guideline “the purposes of trial monitoring are to verify that:a) The rights and well-being of human subjects are protected.b) The reported trial data are…

OverviewThe majority of Clinical Trials are international and run in multiple countries, so in order to make their conduct successful many trial-related documentation needs to be translated, reviewed, and delivered…