Team
TRANSLATIONS TO SWEDISH
The following is an overview of our specialised medical translators who are Swedish native-speakers. They are paired with a trusted colleague with whom they regularly cooperate on projects requiring translation and revision using the four-eyes principle.
Karin Folkeryd
Source languages
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English
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German
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Writing ▪ Linguistic validation ▪ Drawing up glossaries
Specialisms
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Clinical trial documents for patients, such as informed consent/assent forms, patient diaries, patient questionnaires, (e)PROs, (e)COA, patient recruitment materials and lay protocol synopses
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Clinical trial documents for healthcare professionals, such as investigator’s brochures (IBs), research protocols and protocol synopses
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Regulatory pharmaceutical documents, such as summaries of product characteristics (SmPCs), labels and patient information leaflets (PILs)
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Medical device documents, such as instructions for use (IFUs), manuals, summaries of safety and clinical performance (SSCPs), software user guides, standard operating procedures (SOPs) and laboratory manuals
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Legal documents, such as clinical trial agreements and marketing authorisation documents (including DSURs and PSURs)
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Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports
Anna Grynfeld Smith
Source language
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English
Services
Translation ▪ Revision ▪ Implementation of changes ▪ Back-translations ▪ Voice-over directing ▪ Subtitling ▪ Localisation ▪ Drawing up glossaries ▪ Linguistic validation consultancy
Specialisms
Clinical trial documents, such as ICFs, research protocols, patient questionnaires/diaries, investigator’s brochures ▪ Pharmaceutical documents, such as summaries of product characteristics, patient information leaflets, and labels ▪ Patient information videos ▪ Medical reports ▪ Technical documents, such as manuals, guidelines, IFUs, and operating techniques relating to medical devices, medical device software and IVD products
Nina Pettersson
Source languages
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English
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French
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Writing ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (with and without recruitment) ▪ Linguistic sign-off (LSO) ▪ Screenshot reviews ▪ Drawing up glossaries
Specialisms
-
Clinical trial documents for patients, such as informed consent/assent forms, patient diaries, patient questionnaires, (e)PROs, (e)COA, patient recruitment materials and lay protocol synopses
-
Clinical trial documents for healthcare professionals, such as investigator’s brochures (IBs), research protocols and protocol synopses
-
Regulatory pharmaceutical documents, such as summaries of product characteristics (SmPCs), labels and patient information leaflets (PILs)
-
Medical device documents, such as instructions for use (IFUs), manuals, summaries of safety and clinical performance (SSCPs), software user guides, standard operating procedures (SOPs) and laboratory manuals
Malin Algers
Source language
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English
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Linguistic sign-off (LSO) ▪ Subtitling ▪ Electronic implementation/migration ▪ Screenshot reviews ▪ Drawing up glossaries
Specialisms
-
Clinical trial documents for patients, such as informed consent/assent forms, patient diaries, patient questionnaires, (e)PROs, (e)COA, patient recruitment materials and lay protocol synopses
-
Clinical trial documents for healthcare professionals, such as investigator’s brochures (IBs), research protocols and protocol synopses
-
Regulatory pharmaceutical documents, such as summaries of product characteristics (SmPCs), labels and patient information leaflets (PILs)
-
Medical device documents, such as instructions for use (IFUs), manuals, summaries of safety and clinical performance (SSCPs), software user guides, standard operating procedures (SOPs) and laboratory manuals
-
Legal documents, such as clinical trial agreements and marketing authorisation documents (including DSURs and PSURs)
-
Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports