Life Science Translation and Localization Services
Customizable. Accurate. Always On-Time.
Why Choose Us
- Customizable Technology – AI-optimized translation expertise with processes customized to your specific needs.
- Reliable – Our linguists are doctors, scientists and medical experts, ensuring the highest quality outputs, every time.
- Always On-Time – We find unique solutions to ensure timelines are met for each customer, while maintaining 99.7% on-time delivery.
Expertise In
Clinical Research
Pharmaceutical
At Language Scientific, we understand the critical role that precise translation plays in the pharmaceutical industry. Our specialized services ensure that your pharmaceutical documents are accurately translated, facilitating seamless global operations and compliance with international regulations.
Our Pharmaceutical Translation Services Include:
- Clinical Research Documentation: Accurate translation of clinical trial protocols, case report forms (CRFs), and informed consent forms to support multi-country trials.
- Regulatory Submissions: Ensuring that all regulatory documents meet the stringent requirements of authorities such as the FDA, EMA, and PMDA.
- Manufacturing and Packaging Materials: Translating manufacturing processes, batch records, and packaging inserts to maintain consistency and compliance across markets.
- Patient-Facing Materials: Providing clear and culturally appropriate translations of patient information leaflets and educational materials to enhance patient understanding and safety.
Medical Device
At Language Scientific, we specialize in delivering precise and culturally adapted translations for the medical device industry. Our expert team ensures that your documentation meets international regulatory standards, facilitating seamless global market entry and compliance.
Our Medical Device Translation Services Include:
- Operating, Maintenance, and Installation Manuals: Providing clear and accurate translations to ensure proper device usage and maintenance.
- Instructions for Use (IFUs): Translating user guides to meet regulatory requirements and enhance user comprehension.
- Regulatory Compliance Documents: Assisting with translations for European Union and Asian market compliance, including MDR and IVDR requirements.
- Software Application Interfaces and Documentation: Localizing software interfaces and accompanying documentation for global users.
- Package Inserts and Labels: Ensuring that all labeling and packaging information is accurately translated to maintain compliance and user safety.
How we do it
Understanding Your Needs
Tailored Solution Design
Selecting the Right Experts
Leveraging Cutting-Edge AI Technology
Quality Assurance
Seamless Onboarding and Support
Long-Term Relationships With
Real-World Successes
A leading human therapeutics company in the biotechnology industry was working with a German contract manufacturer who needed to document
A major international supplier of secure personal identification systems was bidding on a large international sales opportunity with the Mexican
Solely focused in the life sciences, Language Scientific works closely with many organizations in the healthcare industry in assisting with
A leading medical publishing company required translation of some of their website content into multiple languages. Language Scientific assigned this
A leading diabetes care company and producer of insulin needed patient case report forms translated from Japanese into English as
Help Your Business Grow
Introduction EU Regulation 2017/746 (IVDR) is a regulation enacted in 2017 for releasing in-vitro medical devices into the European Union. It was published in April ’17 and is closely aligned to the EU regulation on medical devices. The IVDR has a significant impact on Medical Devices companies from a language
Introduction In today’s rapidly evolving world of medical clinical research, the requirement for precise and reliable translation services is greater than ever. Here’s a link to a Blog titled “Making Medical Translation A Differentiating Factor For Successful Clinical Trials” that delves into this issue in full detail. With the recent
Introduction The European Union Medical Device Regulation (MDR) adopted in April 2017, changed the European legal framework for medical devices and introduced new principal and supportive responsibilities for EMA and for national authorities in the assessment of certain categories of medical products. The aim of the MDR is to ensure patient safety and
