Once the preclinical phase is complete and you have received approval to run clinical trials, there’s a new set of challenges and milestones to think about.
First up is the technical work, like drafting Investigator Brochures. This document needs to be clear, absolutely accurate, and understandable to all stakeholders.
Then you need to recruit a diverse group of participants, and retain them – two of the biggest challenges in running a successful clinical trial. You need to keep everyone updated, engaged, and safe throughout; manage logistics; gather and analyze data; keep your documentation updated for regulatory submissions; and communicate results to interested parties (e.g., study participants).
It's a lot. But nothing you can’t handle with help from Conversis! We’ve got expert linguists in over 110 countries, covering 330+ language combinations, including regional and rare ones. We can help you to speak to investigators and participants alike – in the right language, and in a way that resonates culturally. We can help translate recruitment materials that attract and retain a diverse audience, manage your multilingual data efficiently, and our regulatory specialists can assist with submissions materials for every major body globally.
