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Launch global clinical programs with ease

Accurate and secure language translations for the life science industry

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.
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Achieve highest quality

Meet regulatory requirements and support the highest levels of content quality

Speed up localization

Accelerate drug submissions, device interfaces, clinical trials, go-to-market campaigns and patient information

Protect your data

Take advantage of centralized control and ISO-certified technology
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.

Centralized content processes

Bring your products to international markets quicker and easier with centralized multilingual processes that streamline the delivery of accurate content to regulatory bodies, patients and medical professionals. Take control of your multilingual dossier submissions, clinical and drug safety documentation, medical information, global labeling and international product launches.

Clinical development

Deliver clinical studies across multiple languages and countries using a translation solution you can trust. Control your terminology with zero deviation from corporate and insurance-approved terms and names. SDL follows the ISPOR task force’s recommendations with regard to linguistic validation of PRO instruments. We also provide a solution from early phase studies through to RCTs, NDA/MAA, brand launches and post-marketing surveillance studies including pharmacovigilance translations.

Global regulatory compliance

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.
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Global pharmaceutical brand launches

Introduce new drugs, products and programs to market smoothly and efficiently with global launch solutions that help marketing professionals with website content, marketing collateral, advertisements, patient adherence material, videos and training. 

Maintain brand integrity with a strict adherence to your company style and tone. Let our desktop publishing and design service handle your creative launch programs and use our unique analytics solution to understand and measure brand awareness in global markets and gain competitor intelligence.

International medical devices

Trust industry experts when launching medical devices to global markets. Let us handle your multilingual communication in an investigational setting, in market. With ISO certification, we adhere to the highest quality and data security standards and we’re supported by leading global standards authorities. We cover regulatory and clinical documentation, medical device patents, operating manuals, software and labeling.

International labeling solutions

Let our pharma labeling solution help you manage the complexities involved in global drug labeling. With simplified processes, all your reviews and comments are tracked, stored and made available for audit and future use. You can also lock down parts of text to avoid unwanted changes. This increases the turnaround time for label changes as it eliminates unnecessary translation or review work not in scope of the required label change.