Medical Writing

Regulatory documents for clinical investigations

We support you in writing all documents required in a clinical investigation or clinical evaluation process. Our experts utilise templates and forms to ensure the completeness and regulatory compliance of these numerous documents.

Publications

We write scientific manuscripts and conference presentations. We start by evaluating the best strategy to use available data for the specific target group.

Read more about our publications services

Examples of our medical writing services

Our broad experience in medical writing includes for example the following:

• Clinical investigation plan / synopsis
• Patient consent documents
• Patient information
• CRFs (case report forms)
• Questionnaires
• Investigator site file (ISF)
• Investigator brochure
• Patient diaries
• Processing of Authorities and Ethics
• Committees checklists
• Registration of clinical studies
• Interim / Final reports
• Publications
• Safety documents
• Marketing materials
• Literature search