Compliance with all national and international regulations and guidelines, as well as an optimal adaptation of the manuscript to the requirements of the respective journal, guarantees the best possible acceptance of your publication.

Scientific and medical texts/documents must show a clear structure, which requires a well-structured working method with a focus on the essential things.

We would be pleased to provide you with the following documents:

  • Abstracts
  • Publication manuscripts
  • Poster
  • Newsletter for communication with your study site
  • PowerPoint presentations
  • Training documents

But also other study documents of all kinds gain in significance and persuasive power through professional preparation and clear structuring. This facilitates cooperation with authorities, ethics committees and study sites.


We will be glad to support you in preparing:

  • Study protocol (Phase I – IV)
  • Observation plan (NIS / PASS / PMOS)
  • Clinical investigation plan (CIP) for medical devices
  • Additional study documents (patient information leaflet, informed consent form, patient diary, etc.)
  • Documents for submission (ethics, competent authorities, etc.)
  • Standard operating procedures (SOPs) - tailored to meet your specific needs
  • Clinical study report
  • Interims reports
  • Non investigational reports
  • Study progress reports

The work with study participants represents a special challenge. If required, we also provide consent forms or patient diaries in "simple language" according to current guidelines in order to avoid communication problems or misunderstandings.