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Standardized process for every step of the way

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Medical Writing

DataClin Team ensures that representation and interpretation of study results are consistent with the study protocol and statistical outputs. Our medical writers are committed to develop high-quality documents that comply with regulatory, journal, or other guidelines in terms of content, format, and structure. We believe that a well-structured protocol is the backbone of a good clinical trial and that a good clinical study report is the mirror reflecting all steps of study planning and conduction in addition to study results.

 

For Medical writing, we provide the following solutions:

  • Protocol Development
  • Informed Consent Form
  • Interim efficacy and safety reports
  • Clinical Study Report (ICH-E3 compliant)
  • Publications (medical writing, editing, graphs and visuals)
  • Medical marketing materials
  • Medical educational materials

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