In the life sciences industry, accuracy is not optional—it’s critical. At Translare, we understand the regulatory, technical, and ethical demands of medical and scientific content. That’s why our language solutions for the life sciences sector combine linguistic excellence with subject-matter expertise and strict compliance standards.
What We Translate & Localize
- Clinical Trial Documentation (Protocols, ICFs, CRFs)
- Regulatory Submissions (EMA, FDA, etc.)
- Medical Device Manuals & IFUs
- Pharmacovigilance Reports & Case Narratives
- Scientific Research Papers & Publications
- Product Labels & Packaging
- Medical Marketing Materials
- Training Modules for Healthcare Professionals
- Patient Education Materials
- Software Interfaces & Apps for Healthcare Use
Who We Work With
- Pharmaceutical Companies
- Medical Device Manufacturers
- CROs & Research Institutions
- Biotech Startups
- Healthcare Providers & Hospitals
- Regulatory & Compliance Teams
- Scientific Publishers
- E-health & MedTech Platforms
Why Translare for Life Sciences?
- Linguists with medical, pharmaceutical, or scientific backgrounds
- Adherence to ISO 17100:2015 and ISO 9001:2015 quality standards
- Compliance with EMA, FDA, and local regulatory terminology
- Terminology management and validated glossaries
- Confidential handling of sensitive data
- Seamless integration with your QA, DTP, or review workflows
- Experience in multilingual regulatory submissions and audits
