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.