Guide to Clinical Investigation Plans & Reports for Medical Devices

Regulatory demands for medical devices are stricter than ever. This guide helps you develop Clinical Investigation Plans (CIPs) and Reports (CIRs) that meet MDR, ISO 14155, and global regulatory standards.

What’s Inside?

• Step-by-step guidance on developing CIPs & CIRs – Learn how to structure your plans and reports for clarity and compliance.
• Key regulatory requirements & best practices – Understand MDR, ISO 14155, and what authorities expect from your documentation.
• Practical tips for study design & compliance – Get insights on risk analysis, study objectives, and essential data collection.

Download now and simplify your clinical investigation process!