Regulatory Services in UAE

The UAE (United Arab Emirates) Ministry of Health and Prevention (MOH) manages all the regulatory procedures concerning pharmaceuticals. It sets the national medical and healthcare guidelines for the UAE. It also leads the healthcare demand throughout the Northern Emirates. As per the Pharmaceutical Law, all medical developments must be reported by the MOHAP (Ministry of Health and Prevention, UAE) before they are imported into the UAE for sale and allotment. A medical development factory must successfully document with the MOHAP before recording its medical developments in the UAE.

As a leading global contender, DDReg’s Regulatory Services in UAE provides on-going support and development of customized strategies during all regulatory phases while keeping track of the most recent regulatory requirements to ensure high quality and timely submissions. We deliver reliable safety measures, ensure risk mitigation, and collaborate with experts to facilitate effortless delivery of product launches, regulatory filing and market authorizations.