The clinical trial setting is changing like never before with a flood of new technologies, regulatory flux, Brexit, the Clinical Trial Regulation coming into effect in 2019 and the constant flow of new innovations. As many of the processes involved in clinical trials are now outsourced, drug trial sponsors and CROs, like those attending the … Continue reading Challenges of Outsourcing in Clinical Trials
Marketing any medical device on a global scale involves a product strategy that requires language translation and localization. Many countries impose directives that require companies to translate product information into the language of the local user. The question for medical device manufacturers is not whether or not they need to translate for their target markets, … Continue reading Medical device translation: how to avoid the most common challenges
Translating medicine packaging and labeling information accurately and appropriately for international markets is a challenge that cannot be faced lightly. Imagine a regulatory affairs manager or lead buyer in purchasing staring down at their desk one rainy afternoon, somewhat concerned about an email from senior management that simply states: find a good medical translation supplier … Continue reading Lost in Translation – Medicine Translation Challenges
These days, hundreds of clinical trials enable pharmaceutical and medical companies all over the world to advance pharmacological knowledge and enhance patient care. Accurate, professional translations of Clinical Trial Protocols (CTPs) are a core element to conducting effective, safe international multi-centre trials: they facilitate the enrolment, treatment and monitoring of a diverse cross-section of participants … Continue reading The Impact of Translations on Clinical Trials
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