Monitoring Medical Device Clinical Trials Effective Monitoring Techniques for Quality Research
Product Details
Take a quick and easy step toward regulatory compliance with this 90-minute Encore presentation — let Lee Truax-Bellows share nearly two decades of real-world, regulated research expertise with you.Lee reveals her unique monitoring strategies that use common sense checklists — giving you the details you need to successfully put your monitoring plans in motion. Plus, you’ll gain a solid understanding of key monitoring issues in medical device clinical trials (and ways to resolve them) — along with take-away tips for better monitoring techniques.
Sign up your entire team to listen in, and you’ll soon be able to:
- Understand the relationship between good clinical practice (GCP) and the monitoring of your medical device trials
- Confidently apply risk management principles to GCPs
- Discover effective monitoring techniques using various checklists for:
- Regulatory document control
- IRB approval
- Device accountability
- Telling the difference between UADEs, adverse events and procedural complications from operator error — and accurately reporting them
- Capturing all potential UADEs
- 100 percent source documentation verification to original source documents
- And more
This distinctive presentation is great for clinical research professionals new to medical devices — and for anyone whose success hinges on a working knowledge of medical device monitoring strategies. Don’t miss your chance! Register today. You’ll have an opportunity to ask your toughest questions during the Q&A session.