Life Sciences
Ensuring You Meet Your Time-To-Market Deadlines
To develop your products and gain regulatory approval, you require complete alignment across your teams. We achieve this through our ISO 17100 certified process, which leverages technical translators, editors and project managers, since 1993.
TYPES
Our Life Sciences translations
Clinical Trials, medical research, medical devices, biotech, health care, and pharmaceuticals
- Study Protocols
- Case Report Forms (CRFs)
- Clinical Outcome Assessments
- Protocol Synopses
- Patient Diaries
- Investigator Brochures
- Patient Records
- Serious Adverse Event Reports
- Summary of Product Characteristics
- Labeling and Packaging
- Patient Information Leaflets (PILs)
- Patient Reported Outcomes (PROs)
- Medicines Summary
- Clinical Study Protocols
- Informed Consent Forms (ICFs)
- Patents and Patent Applications
- Technical Manuals
- Regulatory Documents
- Medical Literature
- Inserts and Packaging
- Patient Files and Correspondence
- Marketing, Advertising, and Websites
- Scientific and Technical Articles
- Patents and other IP Documents
- Patents for Medical Devices
- Patents for Surgical Devices
- Medical Device Graphic UI
- Instructions for Use
- Operating Manuals
- Installation Manuals
- Manufacturing Process Descriptions
- Package Inserts and Labels
ISO-Certified Quality Assurance to Reach Your Markets
Our ISO 17100 certified process is critical to delivering the translations that will drive your projects forward. Cross-border and localization needs that exist to achieve your go-to-market requirements are easily addressed by our translators and project management teams.
Healthcare
