The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process.
The FDA holds companies responsible for filing new 510(k)s when one
change is major enough to impact safety / effectiveness, or when a
series of lesser changes finally reach the "tipping point".
This is a major headache. How can companies make that determination? How
can they trigger such an analysis over the major change or the series
of smaller changes. What approaches are required for product changes;
for process changes. How is the process risk-based? How to maximize the
process against scarce resources. What are the different considerations
for CE-marked product?
Areas Covered in the Session:
- U.S. FDA device clearance / approval
- FDA's and EU's emphasis
- Product changes and filing a new 510(k) - who's responsible
- Tracking and evaluating changes - the "tipping point"
- Is the process "risk based"?
- K-97-1 and the FDA's "Decision Tree"
- Documenting the process / rationale
- Resolving a "wrong decision"
Who Will Benefit:
- Senior Management, Project Leaders, Internal / External Consultants
- Regulatory Affairs
- Quality Systems Personnel / QAE
- R&D and Engineering Staff
- Personnel involved in Lean and Six Sigma Initiatives
- New product development, Regulatory Submissions, Driving company-wide quality initiatives, under a risk-justified approach
- CAPA personnel desiring to minimize post-production / life cycle, root cause investigation, and other costly problems