Team
TRANSLATIONS TO DUTCH (NL)
The following is an overview of our specialised medical translators who are Dutch (NL) 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.
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Jolanda Bijl
Source languages
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English
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French
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Linguistic sign-off (LSO) ▪ Testing apps ▪ Electronic implementation/migration ▪ Screenshot reviews
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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Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports
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Medical marketing, education/training materials and scientific books/articles
Anneke van der Weerd
Source language
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English
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (with and without recruitment) ▪ Electronic implementation/migration ▪ Screenshot reviews
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
Katrien De Clercq
Source languages
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English
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French
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (with and without recruitment) ▪ Linguistic sign-off (LSO) ▪ Testing apps ▪ Electronic implementation/migration ▪ Screenshot reviews ▪ Drawing up glossaries ▪ Voice-over
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
-
Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports
-
Medical marketing, education/training materials and scientific books/articles
Veronique Doggen
Source languages
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English
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French
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Portuguese
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Writing ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (with and without recruitment) ▪ Linguistic sign-off (LSO) ▪ Subtitling ▪ Testing apps ▪ 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
-
Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports
-
Medical marketing, education/training materials and scientific books/articles