Norwegian Medical Translation Services for CROs and Medical Device Manufacturers
Medical and technical translations require absolute precision, industry-specific knowledge, and strict adherence to international standards. We specialize in professional medical translations to and from Norwegian, supporting Contract Research Organizations and medical device manufacturers with secure, ISO-certified language services.
Whether you’re managing clinical studies, submitting regulatory dossiers, or preparing technical files, we ensure that your translations meet the highest standards of accuracy and compliance.
Certified quality and regulatory assurance
We are certified under ISO 17100 for translation quality and ISO 27001 for data security. This means:
- All translations are carried out by qualified linguists with medical or technical backgrounds
- Each project includes translation, independent revision, and final review
- Terminology is consistent, clear, and aligned with regulatory expectations
- Confidentiality and document security are maintained at every step
Our processes are built for the demands of highly regulated environments, including MDR, IVDR, FDA, and EMA frameworks.
Medical and technical expertise
We translate a wide range of documentation for clinical research, product development, and market access.
For CROs:
- Clinical trial protocols, informed consent forms, and patient-facing materials
- Investigator brochures, safety reports, and regulatory submissions
- CRFs, monitoring reports, and site communication
- EMA, FDA, and Helsedirektoratet documentation
For medical device manufacturers:
- Instructions for use (IFUs), technical files, and user manuals
- Product labeling, software interfaces, and digital applications
- Risk assessments, CERs, PMS and PMCF documentation
- Quality management documentation and design history files
Our translators combine linguistic precision with deep knowledge of healthcare, biotechnology, and engineering terminology.
Data security and full confidentiality
Medical and technical documents often contain confidential patient data and proprietary product information. As an ISO 27001-certified provider, we protect your information with:
- Encrypted file transfer and secure cloud infrastructure
- Strict access controls and confidentiality agreements
- Compliance with GDPR, HIPAA, and Swiss data protection laws
We treat your documentation with the same level of protection as you do.
Why leading CROs and MedTech companies work with us
- ISO 17100 and ISO 27001 certified
- Native-speaking medical translators with subject-matter expertise
- Regulatory-ready terminology and formatting
- Fast turnaround times with scalable capacity
- Multilingual support and integration with structured content formats
- Delivery in XML, eCTD, InDesign, PDF, and more
We are a trusted partner for accurate, audit-ready translations—delivered with speed and care.
How it works
1️⃣ Upload your documents via our secure platform or API
2️⃣ Receive a detailed quote with pricing and delivery timeline
3️⃣ We assign your project to an experienced medical translator
4️⃣ Receive the translated documents on time, fully reviewed and ready to submit
Request a quote today
Whether you're submitting to the Helsedirektoratet, launching a device on the Nordic market, or conducting a multi-country clinical trial, we deliver Norwegian medical translations that meet the demands of international regulations.
Upload your documents or contact our team today to receive a free, no-obligation quote—fast, secure, and precise.
Let us support your next submission with confidence and clarity.
