• Clinical Trials Services
  • Clinical Plan
  • Regulatory Affairs
  • Monitoring, Logistics & Quality Control
  • Data Management & Statistics
  • Medical Writing

• Epidemiological studies & surveys

• Staffing Solutions

• Biotechnology & Diagnostics

• Pharmacovigilance

• Patient Education Programs

• Technology & e-Clinical

Medical Writing

Our medical writers have a strong academic, pharmaceutical, and biotechnology industry background and can help you prepare clear, concise, and high quality:

• Investigator Brochure
• Protocol (from Phase II to IV, Epidemiological, Farmacoeconomic, etc)
• Case Report Form
• Patient information leaflets for clinical trials and package inserts
• Informed Consent Form
• Safety data reports
• Statistical analysis plan
• Medical translation services
• Regulatory submissionss
• Final Report
• Scientific articles (English or Local Language)
• Posters and Congress Communications

Moreover, we can help your company with New Ideas and Hypothesis for new clinical trials and observational Studies. That’s what makes us different!

To learn more about this service, please contact us at masinformacion@infociencia.com