DUBLIN--(BUSINESS WIRE)--The "CAPA (Corrective and Preventative Action) Training Course" conference has been added to ResearchAndMarkets.com's offering. This course has been specifically designed for ...

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.

Let’s say, your medical device business has received a complaint from a customer. It happens to all medical device manufacturers and the complaint can range from the relatively minor to severe with ...

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 ...