Biotech & Pharmaceutical Translation Services

Language Intelligence provides ISO-certified biotech and pharmaceutical translation services to help companies successfully enter foreign markets. 

Reliable Biotech and Pharmaceutical Translation Services Needed When Entering Global Markets

From discovery to delivery, bringing a drug to market can be a lengthy and costly process. International biotechnology and pharmaceutical companies face growing regulations as clinical research and drug manufacturing expand globally. Entering foreign markets require end-to-end biotech and pharmaceutical translations for every stage of the product lifecycle, from clinical research and trials to regulatory submissions and product labeling. 

Comprehensive and quality translation will determine how quickly and successfully your product reaches the market and your international consumers. For the past 30 years, Language Intelligence has been providing accurate and reliable biotech and pharmaceutical translation services to help our clients comply with regulatory requirements, mitigate risk, and deliver trustworthy global results.

OVERVIEW

Biotech & Pharmaceutical Content Types

With more than 30 years of experience in the space, Language Intelligence has a sophisticated understanding of the biotech and pharmaceutical industries. Because of our extensive knowledge of regulatory systems and medical terminology, we can ensure reliable translations for the following content types:​

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• Adverse Event Reports

• Case Report Forms (CRFs)

• Genetic testing

• Informed Consent Forms (ICFs)

• Instructions-for-use inserts

• IRB/IEC documentation

• Manufacturing SOPs

• Multimedia audio and visual

• Patents and contracts

• Patient recruitment materials

• Patient surveys and diaries

• Pharmacological studies

• Product information and labeling

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End-to-End Pharmaceutical Translation Services 

Choose Language Intelligence for quality and precise biotech and pharmaceutical translation services. From start to finish, our ISO-certified team of project managers and knowledgable linguists will ensure your translated content meets local regulations, can be clearly communicated to your potential patients, and is ready to enter a global market.  

Quality assurance is extremely important to us, so we only employ native-speaking, in-country linguists who have specialized experience within the biotech and pharma industries. Our end-to-end translation and localization workflow ensure all your content will be up-to-date with the latest compliance and regulatory standards. Plus, for an additional layer of quality assurance, we can provide certified translations and certified translators.