CAPA and Complaint Handling are two systems included in every FDA inspection, and are two of the most frequently cited violations annually.
Questions will focus on:
- FDA expectations
- Compliance strategies that medical device companies should employ
- Pitfalls to avoid
- Inspection strategies in 2014/2015
- How to avoid Warning Letters
This webinar recording is only $129 (AND INCLUDES NATIVE SLIDE POWERPOINT PRESENTATION FILES):
This recording includes a 1 hour Q&A session with retired FDA medical device investigator. He will answer a number of critical compliance questions and concerns related to CAPA & Complaint Handling.
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