Rules, Regulations and Procedures of Formal Registration of veterinary Medicines

Effective drug regulation Medicines are of thepromotes and protects public health by ensuring that :Health professionals and patients haverequired quality, safety and efficacy ;Medicinesthe necessary information to enable them to use medicines rationally ;Illegalare appropriately manufactured, stored, distributed and dispensed ;Promotion andmanufacturing and trade are detected and adequatedly sanctioned ;Access to medicinesadverting is fair, balanced and aimed at rational drug use ;is not hindered by unjustified regulatory work. Natinonal governments are responsible for establishing storng national Drug regulatory authorities (DRAs (with clear mission, solid legal basis, realistic objectives, appropriate organizational structure, adequate number of qualified staff, sustainable financing, access to technical literature, equipment and information, capacity to exert effective market control. DRAs must be accountable to both the govermant and the public and their decision-making processes should be transparent. Monitoring and evaluation mechanisms should be built into the regulatory system to assess attainment of established objectives

کلیدواژه ها:

Drug regulatory authorities ، Registration of veterinary Medicines Formal