Within clinical trial translations, informed patient consent forms (ICFs) are an important and mandatory prerequisite for all submissions that not only represent the patient’s individual rights but also serve as an underlying principle of medical ethics. Under the...
The life science industries are highly regulated for good reason. Without proper guidelines and control mechanisms to ensure safety and quality, dangerous products could be marketed to unassuming customers, making life science translation a necessity for global...
A study participant participates in a clinical trial, contributing invaluable data to understanding the safety and efficacy profile of a drug. Yet, patients, despite risking their lives by participating in a clinical trial, don’t usually get to know the outcome of the...
From May 23-25, CSOFT’s CSOFT Health Sciences’ Life Sciences Unit attended and exhibited at the 10th DIA China Conference held at the Beijing International Convention Center. This year’s event attracted thousands of pharmaceutical R&D professionals from...
As the demand for quality affordable translations is ever increasing, companies are increasingly harnessing artificial intelligence (AI), moving beyond traditional translation memory and terminology management systems. When using artificial intelligence (AI) for...
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