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Regulatory Writing Services for Drug Approval

• Investigational drug brochures
• Study protocols
• Integrated clinical/statistical study reports (Phases 1-4)
• Integrated summaries of efficacy and safety
• Clinical data summaries and expert reports
• Other regulatory documents for drug approval
• Patient narratives

Other Medical Writing Services

• Literature reviews
• Manuscripts for submission to biomedical journals
• Monographs
• Technical reports for marketing and venture capital efforts