Les résultats finaux d'une évaluation indépendante du programme d'examen des dispositifs médicaux de la Food and Drug Administration des États-Unis ont été publiés, donnant de bonnes notes à celle-ci pour ses efforts visant à améliorer les processus d'examen.
The final results of an independent evaluation of the US Food and Drug Administration’s medical device review program have been published, giving the agency high marks for efforts to improve review processes.
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.
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.