Jun 4, 2014
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.
Medical device manufacturers selling in Egypt will have a six-month grace period before CAPA begins requiring ISO 13485:2012 compliance for registrations and importation.
Egypt’s Central Administration for Pharmaceutical Affairs (CAPA), the country’s medical device market regulator, has published a series of updates and amendments to its registration req
The Central Administration for Pharmaceutical Affairs (CAPA), Egypt’s medical device market regulator, has published a list of approved reference countries that companies applying for market authorization in Egypt may leverage in their device registration efforts.