Team
TRANSLATIONS TO GERMAN (DE)
The following is an overview of our specialised medical translators who are German (DE) 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.
Kathrin Kunze
Source languages
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English
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Swedish
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Latin
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Writing ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (with and without recruitment) ▪ Testing apps ▪ Screenshot reviews ▪ 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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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
Ulrike Nichols
Source language
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English
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Back-translations ▪ Harmonisation ▪ Testing apps
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
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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
Susanna MacKenzie
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 (without recruitment) ▪ Linguistic sign-off (LSO) ▪ Electronic implementation/migration ▪ Screenshot reviews ▪ Drawing up glossaries ▪ Transcription
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
Anita Müller
Source languages
-
English
-
French
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Back-translations ▪ Testing apps ▪ 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