divendres, 6 de juny del 2014

Updated ISO 13485 Requirements from Egyptian Ministry of Health




The Emergo Group Blog provides short updates on quality and regulatory topics that may be of interest to QA/RA professionals in the medical device and IVD industry. No fluff, just straight to the point. We hope you'll enjoy the content.





Staff changes at Indian regulator could boost review processes in the long term

By Stewart Eisenhart, Emergo Group


Egyptian medical device market regulators at the Central Administration of Pharmaceutical Affairs (CAPA) will soon require the latest version of the ISO 13485 standard for quality system compliance, Emergo Group's Cairo office has learned.




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