Designing and Monitoring Approvable Medical Device (cardiovascular) Protocols 2016 is a seminar that covers topics such as:
- Regulations and project management
- Medical devices and purpose of testing and experimentation
- Designing a protocol, meetings and writing
- Organizations: people and processes
- CBP and FDA computer programs
- Consents, statistics, data management
- Device safety reports and adverse events tracking
- Monitoring trips and reports
- Statistical analysis and reports
- Data based management, queries and errors
- Medical Summaries
Designing and Monitoring Approvable Medical Device (cardiovascular) Protocols 2016 brings together:
- Nurses
- Scientists
- Clinical Research Associates (CRAs)
- Pharmacists
- Medical Directors
- Medical Monitors
- Project Managers
- Statisticians
- Regulatory
- Quality
- Administration
- Manufacturing and Labeling