by Dr. Sofia Petrescu | Jul 24, 2026 | Manufacturing, Medical
Are you looking to take your pharmaceutical products into new markets? Every drug that enters a new country brings a documentation requirement with it. Labels, patient information leaflets, regulatory submissions, and pharmacovigilance reports all need to be accurate...
by Dr. Sofia Petrescu | Jul 24, 2026 | Lifescience, Translation
Translation memory gives life sciences companies a strong foundation for efficient and consistent translation. It helps teams reuse previous work, reduce repeated effort, control costs, and maintain continuity across document versions. For regulated industries,...
by Dr. Sofia Petrescu | Jul 2, 2026 | Translation, Medical
Clinical trials run on tight timelines, and all key documents must be translated, reviewed, and approved before studies can begin. Delays in translation can delay the entire trial, especially across multiple countries. Clinical trial documents are highly regulated. A...
by Dr. Sofia Petrescu | Jun 10, 2026 | Medical
Managing product information across EU markets is time-consuming. Every approved change triggers translation updates, artwork revisions, and packaging reprints across up to 24 language versions. Electronic Product Information (ePI) offers a different approach. Instead...
by Dr. Sofia Petrescu | May 22, 2026 | Medical
Most life science companies tracking the EU AI Act amendments have been focused on the high-risk AI documentation requirements, the technical files, instructions for use, and database registrations. In April, those deadlines were pushed back to 2027 and 2028. What did...
