Food and Drugs (Registration, Licensing and Inspection) Regulations, 2017. Country/Territory Belize Document type Regulation Date 2017 Source FAO, FAOLEX Long titleRegulations made by the Minister responsible for health in exercise of the powers conferred upon him by section 55 of the Food and Drugs Act, Chapter 291 of the Substantive Laws of Belize, Revised Edition 2011 and all other powers thereunto him enabling. Subject Food & nutrition Keyword Business/industry/corporations Certification Enforcement/compliance Consumer protection Food quality control/food safety Drugs Inspection Liability/compensation Offences/penalties Procedural matters Registration Geographical area Americas, Central America, Latin America and the Caribbean, Small Island Developing States Abstract This Regulation sets forth procedures and principles of registration, licensing, inspection, confiscation or destruction, revocation and cancellation of licenses, application for importation authorization for orphan drugs, grant or refusal of license, application for amendment of product license, application for facility license, and notification of changes in businesses and ownership. The form for an application for registration of a drug is set out as Form 1 in Schedule 1 and the form for an application for facility license is set out as Form 2 in Schedule 1. This Regulation underlines that a facility licence shall not be transferred to any other person or facility. This Regulation prohibits the sale of unregistered and unlicensed drugs. Furthermore this Regulation sets forth provisions on duties and authorities of competent institutions, inspectors, duration and renewal of product and facility licence, liabilities of product licensee, and offences and penalties. Full text English Website www.health.gov.bz