How the EU AI Act is Reshaping Innovation in Healthcare Products
The healthcare product sector is experiencing a technological transformation like never before. Algorithms analysing radiology images, natural language models summarising complex clinical records—the use of artificial intelligence (AI) is no longer a future promise but a central driver of operational efficiency. Yet the introduction of
AI-generated voice-over has rapidly evolved from a technological curiosity into a practical operational resource within the communication strategies of many organisations in the healthcare sector. At the same time, the debate around its use has intensified and become increasingly polarised. On one side, pharmaceutical brands
The Risks of Using AI in Regulatory Dossier Translation: Hallucinations and Critical Errors
AI is rapidly reshaping how life sciences organisations work — and translation is no exception. Faced with ever-growing submission volumes, compressed timelines and global programmes that rarely run sequentially, many Regulatory Affairs teams are understandably asking the same question: can AI help us translate faster, and still submit with confidence? The short
5 hybrid strategies: machine translation + human review for healthcare regulatory compliance
Healthcare and Life Sciences companies are under growing pressure. Demand for language services in this sector is rising by around 9.5% per year, driven by regulations such as the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR). The result? Large volumes of
Using AI for Translation: Stay MDR-Compliant
Are you using Machine Translation or AI to translate medical device documentation? Wondering whether that could lead to non-compliance with Regulation (EU) 2017/745 (MDR)? Here’s what you need to know.
Understanding Med-PaLM: Google’s Generative AI in Healthcare
Med-PaLM, a groundbreaking large language model (LLM) developed by Google, signifies a significant advancement in the application of artificial intelligence (AI) within the healthcare sector. Trained specifically with a vast corpus of medical data, Med-PaLM aims to revolutionize the way medical professionals access and interpret
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Other services
Pharmaceutical translation: why precision can determine a product launch
A clinical trial can take years to generate robust results. A regulatory submission may go through months of assessment. And yet, all that work can be delayed for a reason that rarely makes headlines: a poorly managed pharmaceutical translation. In the pharmaceutical industry, translation is not a last-minute administrative task. It is the link between science, regulation and market access. When it fails, the
