The regulatory authorization of a medicinal product. The regulatory authorization of a medicinal product. If the element is present, it must have either a @value, an @id, or extensions Business identifier for the marketing authorization, as assigned by a regulator. The medicinal product that is being authorized. The country in which the marketing authorization has been granted. Jurisdiction within a country. The legal status of supply of the medicinal product as classified by the regulator. The status of the marketing authorization. The date at which the given status has become applicable. The date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored. The beginning of the time period in which the marketing authorization is in the specific status shall be specified A complete date consisting of day, month and year shall be specified using the ISO 8601 date format. A period of time after authorization before generic product applicatiosn can be submitted. The date when the first authorization was granted by a Medicines Regulatory Agency. Date of first marketing authorization for a company's new medicinal product in any country in the World. The legal framework against which this authorization is granted. Authorization in areas within a country. Marketing Authorization Holder. Medicines Regulatory Agency. The regulatory procedure for granting or amending a marketing authorization. The regulatory authorization of a medicinal product. The assigned number for the marketing authorization. Country of authorization. Jurisdiction within a country. The legal status of supply in a jurisdiction or region. The start and expected end date of the authorization. The regulatory authorization of a medicinal product. Identifier for this procedure. Type of procedure. Date of procedure. Applcations submitted to obtain a marketing authorization.