Burlington, Massachusetts / Syndication Cloud / February 15, 2026 / Alpha Software Key Takeaways Eliminate Backlogs: ...

For two years running, corrective and preventive action (CAPA) problems have been the most cited FDA Form-483 deficiency during inspections of medical device manufacturers (see the “Recent FDA ...

This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements. Details Discount : Get 15 % Discount as a early bird ...

CAPA systems have come under intense scrutiny by the FDA in recent years. This course will examine the current industry-FDA environment and will give you tools for survival; it will provide a ...