Practical Issues with Conducting Multi-National Clinical Trials for Medical Device Approval in the US 2012 is a webinar that covers topics such as:
- Comparison of US and non-US regulatory processes for medical device clinical trials
- Essential elements of medical device clinical trials: Device, protocol, sites, data
- Clinical trials with devices approved in other countries
- Concerns with non-US clinical data
- Using non-US clinical experience: retrospective data analysis
- Managing US-based and international clinical investigators
Practical Issues with Conducting Multi-National Clinical Trials for Medical Device Approval in the US 2012 brings together:
- Clinical trial professionals: project managers, CRA, and site coordinators
- Investigators in medical device clinical trials
- QA/QC/Compliance/Regulatory affairs professionals
- Clinical trial specialists
- People investing in FDA-regulated product development projects
- Senior management executives (CEO, COO, CFO, etc)
