Medical and Technical Writing

Create Key Informational Tools for Your Business

GBC offers flexible arrangements to support your medical and technical writing needs. GBC medical and technical writing services include:

Clinical Trial Related Materials

  • ICH-GCP Compliant Clinical Study Protocols and Amendments
  • Model Patient Informed Consent Forms (ICFs)
  • Site Recruitment and Qualification Questionnaires (SRQs)
  • Description of Study (DOS)
  • Clinical Trial Management Plans, including:
    • Clinical Site Development and Management Plans
    • Data Management Plans
    • Biospecimen Management Plans
    • Study Monitoring Plans
    • Study Close Out Plans
    • Adaptive Trial Transition Plans
  • Case Report Forms (CRFs) and Instructions
  • Investigator Brochures (IBs)
  • Project Summaries
  • Study Schematics, Work-Flow, and Process Diagrams
  • Tabular Summaries
  • Patient Narratives
  • Pre-Clinical Reports
  • Clinical Trial Reports

Scientific Materials

  • Abstracts, Manuscripts and Journal Articles
  • Grant Applications
  • Literature Reviews
  • Scientific Posters

Business Documents

  • Business Plans
  • Project and Business Proposals
  • Requests for Proposal (RFPs)
  • Contract Key Terms
  • Presentations for Investors, Customers, and Conferences
  • Marketing Collateral
  • Web Site Content and Electronic Media

For additional information on GBC’s consulting services please contact consulting@globalbioclinical.com or register and send us your inquiry here.