DE

Medical Writing Service

How we meet the needs of your audience

Our medical editors type with great enthusiasm, but never lose sight of their primary goal: to produce concise, understandable, and well-structured documents for your study or submission. They prepare or revise any clinical study document, tailored to your needs and specific requirements, in compliance with the most up-to-date guidelines and international standards.

Whether you require a short summary or a comprehensive clinical trial report, our writers will deliver on time and with precision. Regardless of the type of document, everything is proofread to ensure the highest quality. Our medical writers have the scientific knowledge and skills to summarize and explain complex contents to the audience of your needs!

What we do in the Medical Writing department

  • We write the entire spectrum of regulatory documents including – but not limited to – study protocols and study reports, investigator’s brochures, subject information and consent forms, investigational medicinal product. dossiers, summaries for submission dossiers, and briefing books, as well as publication manuscripts, conference posters and presentations.
  • We review and optimize all types of documents e.g., clinical expert reports, standard operating procedures, manuals, and guidelines.
  • We always double check!

    • Andreas Klostermann, SelectIon

      CSO

      "As an innovative biotech company in an early phase of clinical development, we require a professional and flexible CRO to manage our complex studies. In FGK we have found an outstanding CRO partner that is able and willing to optimize and customize their processes to our specific needs. FGK’s highly experienced and responsive team ensures that challenges of our projects are always adequately addressed and managed timely.”