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Ordinary Passport (Spanish: Pasaporte ordinario) – issued for ordinary travel, such as vacations and business trips; Collective Passport (Spanish: Pasaporte colectivo) – issued for the occasion of pilgrimages, excursions and other acts of analogous nature, whenever reciprocity with the destination country exists; its validity is limited a single trip, whose duration will not be able to ...
The Spanish Agency of Medicines and Medical Devices (Spanish: Agencia Española de Medicamentos y Productos Sanitarios; AEMPS) is a regulatory and autonomous agency of the Government of Spain that acts as the highest sanitary authority in the country in terms of medical safety on medicines, health products, cosmetics and personal care products.
Authorization is the responsibility of an authority, such as a department manager, within the application domain, but is often delegated to a custodian such as a system administrator. Authorizations are expressed as access policies in some types of "policy definition application", e.g. in the form of an access control list or a capability , or ...
An electronic visa (E-Visa) and an electronic travel authorization (ETA, also styled eTA) are digital travel permits commonly required in conjunction with a valid passport for entry into specific jurisdictions. These electronic travel documents have gained prominence in the modern era of digital connectivity and streamlined travel processes.
In Spain, a driving licence is an official document which authorises the holder to operate motor vehicles.It is issued by the Directorate-General for Traffic (DGT). [1]As Spain is a member of the EU and EEA, Spanish driving licences are European driving licences, adhering to Directive 2006/126/EC, and are valid throughout the European Economic Area.
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The Federal Commission for Protection against Health Risks (in Spanish, Comisión Federal para la Protección contra Riesgos Sanitarios, Cofepris) is a regulatory body of the Mexican government.
An Emergency Use Authorization (EUA) in the United States is an authorization granted to the Food and Drug Administration (FDA) under sections of the Federal Food, Drug, and Cosmetic Act as added to and amended by various Acts of Congress, including by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), as codified by 21 U.S.C. § 360bbb-3, to allow the use of a ...