September 20, 2024—We are excited to announce the release of the Guide to Sponsor-Investigator Management of Multisite Studies! Successfully managing a multicenter study under an Investigational New Drug (IND) or Investigational Device Exemption (IDE) application demands meticulous planning and execution. This guide is designed to assist Principal Investigators in navigating each phase of their study with precision and adherence to regulatory standards.
From initial planning to final reporting, our guide offers valuable insights and practical tips for how to operate your multicenter study efficiently and compliantly. Whether you’re an experienced investigator or new to the field, this resource will support you in achieving successful outcomes in your research.
Key Features:
- Guidance on planning and executing multicenter studies
- Practical tips for maintaining regulatory compliance
- Strategies for effective communication and coordination across sites
- Insights into best practices for data management and reporting
Empower your research with the knowledge and tools you need to succeed!
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