We work with your team and subject matter experts to develop a data-driven messaging strategy for your program across all documents. This approach ensures document users, whether clinical decision makers or regulatory approvers, have quick access to the product information that is most relevant to their needs.
Clinical Medical Writing Solutions to Meet
Your Research Needs
• Protocols and Amendments
• Instructions for Use
• Investigator Brochures
• Informed Consent Forms/HIPAA
• Financial Disclosure Forms
• Clinical Trial Investigator Agreements
• CEC and DSMB Charters
• Statistical Analysis Plans
• Study Plans including Data Management, Monitoring, Safety
• Interim and Final Study Reports
• Annual Regulatory Reports
• Publication Strategies and Publication Assistance
Why Choose GLOBAL Medical Writing?
Transparency, accuracy, and quality are paramount to the success of clinical trials and regulatory submissions. Our Medical Writing Team works closely with Sponsors, the clinical trial team, and our biostatisticians to transform data into an accurate and evidence-based account that represents the full scope of clinical trials.