1. A national database for Medical Products shall be established in the EDE, in which all data and information related to Medical Products, their technical specifications, pricing and other data shall be recorded and stored. 2. Determined by a decision of the BOD. The sources of this data and information, and the controls and procedures for recording, storing, managing, using, circulating, exchanging and making it available to the Ministry, the Competent Health Authorities, the public, health professionals, health and Pharmaceutical Establishments, and biobanks, and the mechanisms for linking them to the relevant databases in all health and relevant authorities, and the obligations of these authorities to provide the EDE with any relevant data and information available to them or to the Establishments affiliated with them.
Interpretation and application must be checked against the official text and current version.