Our medical translation services for the Life Sciences, Pharmaceutical and Healthcare industries cover everything – from global clinical trials, medical affairs, drug safety and labelling to product launch and marketing.
Quality and accuracy are everything when it comes to medical translation and translating medical terminology and industry-specific terms for the Pharmaceutical, Healthcare and Biotechnology industries.
We have been supporting pharmaceutical, biotech, and medical device companies as well as CROs, CTOs and Healthcare providers for over 14 years now on all content aspects, including:
- Manuals, User Guides and IFUs (Instructions for Use)
- Labelling, Packaging & Inserts
- EDC (Electronic Data Capture) for Web and Handheld Interfaces
- Patents, IP (Intellectual Property) & Contracts
- Medical Forms & Records
- SOPs (Standard Operating Procedures)
- Protocols, Case Reports & Patient Diaries
- PRO (Patient Reported Outcomes) & ePRO Content
- Text and Recording for IVRS (Interactive Voice Response Systems)
- Fully Documented Processes for CFR Part II Compliance
We are fully compliant with the translation quality standard ISO 17100, a prescriptive standard for the entire translation process, governing technology and the qualifications and expertise of linguistic and non-linguistic staff.
Regulatory and compliance issues within these industries mean that you can’t afford to take risks when sourcing medical translators or choosing a medical translation provider. At translate plus, we use industry-specific processes, software and medical translators to ensure the required quality results for this highly specialised sector.