Specialist support across clinical research, Clinical Outcome Assessments (COAs) and medical device regulatory content.
Clinical Research
From early COA planning and COA licensing and management to Linguistic Validation and eCOA migration support, we help clinical trial sponsors, CROs, COA licensing companies and eCOA providers coordinate complex requirements across global studies.
Linguistic Validation is at the core of our clinical research work. Within our ISO-certified quality framework, we manage complex multilingual Linguistic Validation workflows and can coordinate them alongside the translation of protocols, informed consent forms, patient-facing materials and other clinical trial documentation, supporting consistency across the wider study.
Medical Devices & IVDs
We help medical device and IVD manufacturers prepare clear, consistent multilingual content for international markets through IFU content optimisation and regulatory support, specialist translation, and readability and usability testing.
Why NN Translations
200+
languages
16+
years of experience
11+
years of Linguistic Validation expertise
ISO 9001
& ISO 17100
certified
Resources
Access practical guidance, case studies and supporting materials across our specialist areas.
Workflows, clinician review, cognitive debriefing and participant recruitment.
Explore Linguistic Validation Resources →
Licensing, permissions, instrument versions, translation availability and copyright holder requirements.
Explore COA Licensing Resources →
eCOA migration, implementation support, linguistic review and Screenshot Review.
Explore eCOA Resources →
IFU optimisation, regulated content and translation workflows.
Explore Medical Device & IVD Resources →
Testimonials
“We have worked with Nataliya for more than a decade and continue to entrust our linguistic validation projects to her and the NN Translations team. Their specialist expertise, methodological understanding and reliable project coordination give us confidence that every project will be managed with care, accuracy and close attention to conceptual equivalence, intended meaning and cultural appropriateness.”
Clinical Trial Team Leader
Global Clinical Trial Sponsor
“NN Translations has become a trusted partner for our medical device projects. Beyond delivering accurate translations, their understanding of medical device regulatory requirements enables them to offer proactive advice, improve our documentation workflow and help us meet our compliance obligations. As a scale-up company launching a new product, their support has given us valuable peace of mind. Their flexibility, responsiveness and attention to clarity and consistency have also helped us stay on track with our launch timeline and prepare confidently for international markets.”
Regulatory Affairs Manager
Regulatory Affairs Management | Broncus Medical | Medical Device Manufacturer
Talk to us about your clinical research, COA/eCOA or medical device requirements.