health & life sciences

February 5, 2021

Case study: Medical translation & keyword research

medical device translation
Executive Summary The client, a leading supplier of innovative medical devices for imaging, surgical, and radiation therapy professionals, required translated content to support international sales growth. They came to Scriptis for medical translation and keyword research. Scriptis translated instructions for use (IFUs) and website content […] (Read more...)

April 30, 2021

Case study: Linguistic validation of IFUs on a tight deadline

Executive Summary The client, a manufacturer of laser therapy delivery devices, needed three user manuals translated into eight European languages. Devices sold in the European Union need to demonstrate full compliance with EU-MDR regulations. Therefore, translations for labeling and instructions for use (IFUs) require linguistic […] (Read more...)

April 13, 2021

Case study: Global employee outreach for a pharmaceutical manufacturer

Executive Summary Our client, one of the world’s leading pharmaceutical and biotechnology companies, produces vaccines and pharmaceuticals for human and animal health. In addition to headquarters in Germany, the company also operates subsidiaries and sales offices in Canada, China, Denmark, France, the Netherlands, Spain, and […] (Read more...)

January 6, 2021

Case study: Translation services for clinical trials

translation services for clinical trials
Executive Summary Our client provides software development, consulting, and training for medical and life sciences research. They came to Scriptis requesting translation services for clinical trials. Specifically, training modules for a pharmaceutical trial required translation from English into Japanese. The purpose of the clinical trial was […] (Read more...)

March 23, 2021

Translation for EU MDR compliance

EU MDR Translation
Translation for EU MDR compliance The European Union Medical Devices Regulation (EU MDR) is now in effect. Manufacturers will need to comply with more stringent requirements for medical device labeling and instructions for use (IFUs). Medical device content must be translated into the official language(s) […] (Read more...)