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Google review (SL), 3 months ago
Translated from Dutch
Clinical trial documents, Norwegian Medicines Agency submissions, pharmaceutical dossiers, and patient materials all pass through Norwegian medical specialists. We translate each one accurately.
Norway participates actively in European clinical research and has its own medicines regulatory authority, the Norwegian Medicines Agency (Statens Legemiddelverk), which operates within the EMA framework but with specific national requirements. Norwegian patient-facing materials must be written in clear, natural Norwegian for both Bokmal and Nynorsk variants where relevant.
Our Norwegian medical translators hold degrees in medicine, pharmacology, or life sciences and are fluent in Norwegian regulatory and clinical documentation standards.
Spoken support for medical conferences and staff training is covered too, with interpreting services working between Norwegian and English. Medical records, discharge summaries and vaccination records bound for a state health department or the European Medicines Agency are a separate case, and certified translations can be ordered with the rest of the project. The recipient sets the requirements, so share them early.
In-depth knowledge of Statens Legemiddelverk submission requirements for drug registration and medical device authorization within the EMA framework.
Translation, editing by a second Norwegian medical linguist, and a final terminology check against validated Norwegian medical glossaries.
Patient materials and public health documentation produced in Bokmal by default, with Nynorsk versions available when required.
Patient information leaflets and informed consent forms reviewed for accuracy and clarity for Norwegian-speaking patients.
“I had a pleasant working relationship with BeTranslated. It's a professional translation agency with strong SEO expertise. Communication was clear and they were +”
Google review (SL), 3 months ago
Translated from Dutch
“A proactive company, willing to help. I recommend them for website translation and SEO in multiple languages. In my case it was with the WPML plugin.”
Google review (SL), 2 months ago
Translated from Spanish
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Google review (SL), 10 months ago
Yes. We produce Norwegian-language regulatory documents for Statens Legemiddelverk, meeting the Agency's requirements for drug registration and medical device marketing authorization within the EMA framework.
Yes. We produce medical translations in Bokmal as standard, which is used by the majority of Norwegian speakers. Nynorsk versions are available upon request for documents requiring both official written standards.
Yes. We coordinate Norwegian clinical trial translation as part of multi-country Nordic or European studies, ensuring consistent terminology across all language versions.
Norway follows the EU GDPR via the EEA Agreement, enforced nationally through the Norwegian Data Protection Authority (Datatilsynet). Patient records, clinical data, and any personal health information processed during a translation project are handled under strict GDPR-equivalent safeguards. Files are transferred via encrypted channels, access is restricted to the assigned translator and reviewer, and all project data is deleted after final delivery unless a retention agreement is in place.
Yes. While the majority of Norwegian regulatory submissions to Statens Legemiddelverk use Bokmal, patient-facing materials distributed in certain regions may require Nynorsk versions. We manage both variants within a single project workflow, applying consistent medical terminology across both written standards and flagging any Bokmal-to-Nynorsk adaptation choices for client review.
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