CROs
Tailored Translation Solutions for CROs
NN Translations provides tailored translation and linguistic validation in life sciences for Clinical Research Organizations (CROs), covering essential documents such as informed consent forms, trial protocols, patient diaries, study reports, and patient recruitment materials. With a focus on accuracy, cultural relevance, and compliance with international regulations, we support CROs in conducting seamless international trials.
Our expertise in linguistic validation in life sciences ensures that patient-facing materials and clinical outcome assessments retain their intended meaning across languages and cultures, enabling reliable and comparable data collection across study sites.
We provide CROs with a robust support system, including skilled linguists, expert project managers, and cutting-edge translation tools, to optimize their clinical research projects.
How We Support CROs:
Regulatory Compliance
Ensure translations and linguistic validation in life sciences meet regulations
Pharmacovigilance
Translate for adverse events, ensuring compliance
Specialised Linguistic Expertise
Provide precise, clinically experienced translations
Confidentiality and Security
Rigorously protect trial data
Efficient Project Management
Ensure timely delivery with advanced technology
Patient Recruitment
Enhance trial reliability
Our Services:
- Linguistic Validation of COAs
- Informed Consent Forms (ICFs)
- Clinical Trial Protocols
- Patient Information Leaflets (PILs) and Diaries
- Case Report Forms (CRFs)
- Clinical trial legal content
- Protocol Synopsis
- Patient Card
- Adverse Event Reports
- Site User Guide
- Regulatory Documents
- Study Drug Labels and Packaging
- Linguistic Validation of COAs and Patient-Reported Outcomes (PROs)
- Patient Recruitment materials
What Our Clients Say
