Launch new medical products and programs into international markets without ever compromising on quality and safety. The SDL Life Science Language Platform enables pharmaceutical and medical device companies to take their clinical programs global through streamlined regulatory approval as part of the localization process, while enabling safety monitoring and reporting at any stage.Contact us
The SDL Life Science Language Platform is a fully-integrated solution designed to reduce the cost and remove the complexity from creating multinational pharma and medical device content.
Submit your product information accurately the first time around and protect your revenue, reputation and future medical ventures. Meet stringent regulations whether filing an IND/CTA to initiate further research or NDA/MAA for market approval. We have extensive experience of translating regulatory labels, summaries of product characteristics (SmPC), product information leaflets and modules of the CTD/eCTD. We can also take care of your quality review of documents (QRD) templates and the phrasing required for submission to the bodies of the EMA in accordance with Directive 2001/83/EC.Learn More