Taking careful, early stock of a study’s scope, including what the plan is and what is required for each of the questionnaires and languages, will prevent delays.
TORONTO (PRWEB) September 28, 2020
With increasing pharma, regulatory, and public interest in patient reported outcomes, the use of electronic patient reported outcome (ePRO) tools for clinical research is on the rise. For global clinical trials, the patient-completed questionnaires must be translated. Depending upon the number of languages required, costs may increase and timelines may swell. In this webinar, leaders from Clinical Ink and TransPerfect will discuss approaches to ePRO translation that keep time and expense to a minimum. Across the industry, ePRO translation is an iterative process involving many rounds of amendments from translators, ePRO vendors and customers. This convoluted process squanders time and resources. Taking careful, early stock of a study’s scope, including what the plan is and what is required for each of the questionnaires and languages, will prevent delays. A great translation relationship with a top-tier ePRO provider and translation provider will ensure that translation activities flow as smoothly as possible and customers benefit from ongoing provider improvements to the ePRO translation workflow.
Join Tracey Larrow, Director of Translation and Localization Services, Clinical Ink and Elsa Lindstrom, Project Lead for eCOA-Specific Technology, TransPerfect in a live webinar on Thursday, October 8, 2020 at 11am EDT (4pm BST/UK).
For more information or to register for this event, visit How to Minimize Time and Cost of ePRO Translation.
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