How to Format a Succinct and Comprehensive 510(k) Submission 2012 is a webinar dedicated to
- (k) regulatory requirements
- Changes in 510(k) program
- Systematic methods to increase 510(k) submission quality
- (k) submission requirements for medical devices and in vitro diagnostic devices
- Instructor`s unique 510(k) strategy guide
- (k) formatting in a succinct and comprehensive manner ready for submission
How to Format a Succinct and Comprehensive 510(k) Submission 2012 brings together:
- Personnel involved in clinical affairs (associates, specialists, coordinators, managers and directors)
- Personnel involved in regulatory affairs (associates, specialists, managers, and directors)
- Personnel involved in research and development (associates, scientists, managers, and directors)
- Personnel involved in quality assurance, quality control and quality systems (associates, specialists, engineers, managers, and directors)
- Other interested stakeholders (upper management personnel)
- Site managers, and consultants
