PRODUCT DEVELOPMENT SERVICES
Medical Writing and Publishing

ICON Development Solutions writing expertise supports all phases of development, with contributions and reviews performed by our internal experts in multiple scientific/regulatory disciplines as appropriate. This ensures quality, regulatory-ready documents:
  •    Regulatory submissions, including paper and electronic CTDs
  •    Clinical study reports
  •    Clinical study protocols and amendments
  •    PK and toxicology reports
  •    Manuscripts for publication in biomedical journals
  •    Investigator brochures
  •    SAE narratives
  •    ISSs and ISEs
  •    Executive summaries
  •    Meeting abstracts, posters, and slide presentations
Additionally, ICON offers preparation of electronic reports and regulatory submissions using industry-recognized tools such as Documentum, Core Dossier and ISI Toolbox.