How do you get your medical device through complex clinical trial obstacles and past the finish line? In this eBook, you’ll receive guidance from industry experts with decades of experience in study design, clinical trial operations, data management, and eClinical technology.
The market is ripe for new medical devices, with FDA approvals growing rapidly for this segment. However, new trial complexities and increasing regulatory obstacles mean navigating clinical research can be tough. This resource is a guidebook with field-tested strategies to help you plan your clinical trial roadmap for a more seamless submission.
In the eBook, you will learn about:
- Select regulatory trends affecting medical device studiesÂ
- Best practices for protocol development, data collection, and trial operations
- Must-have tools to incorporate in your medical device clinical trial
Contributing Experts at Medrio:
- Rod McGlashing, Data Science Subject Matter Expert
- Tina Caruana, Director of eClinical Solutions