Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Corrective Actions Preventive Actions - CAPA 101 (Aug 14, 2025)" training has been added to ResearchAndMarkets.com's offering. Corrective ...

DUBLIN--(BUSINESS WIRE)--The "3-Hour Virtual Seminar on Root Cause Analysis, CAPA and Effectiveness Checks" webinar has been added to ResearchAndMarkets.com's offering. This comprehensive course ...

Over years of working with medical device companies, we’ve found that there is a particular area that is often rife with issues for companies — CAPA (Corrective Action and Preventive Action). We see a ...

Establishing a corrective and preventive action (CAPA) system is a quality system regulation (QSR) requirement for medical device firms marketing products in the United States. Although FDA has always ...

Compliance Implementation Services (CIS), a pharmaceutical compliance consulting firm, announced the publication of its white paper on compliance-focused approaches to establishing an efficient, ...

This past August, FDA issued a warning letter to Soleetech Corp., a Taipei, Taiwan-based manufacturer of airway connectors. The agency was not impressed with this organization’s level of compliance.

(MENAFN- GlobeNewsWire - Nasdaq) Opportunities lie in developing efficient CAPA systems for pharma and medical device industries, enhancing root cause analysis, implementing effective solutions, and ...