The Healthcare Products Regulation project recognizes the need to ensure the effective use, safety, and quality of healthcare products and medical devices for the public and health sector. This will be achieved by enhancing the related healthcare regulation and introducing a medical device registration unit. A national formulary and drug coding system is also planned. The project will align a broad range of stakeholders from the regulatory health authority [MoPH] to government healthcare facilities and academic institutions, private providers and other related groups and industries.
As the National Health Strategy Program 2011-2016 draws to a close, project information is currently being updated and will be available in the coming weeks.
An expanding collection of topic related documents and publications, reports and studies.
A sharp drop in the prices of medicines in Qatar over the past two years has come as a great relief to citizens and expatriates, apparently drawing more customers to private pharmacies. A large ...
Links to key project stakeholders, and other health, education, and research institutes.