Production and distribution of veterinary medicinal products | Proizvodnja i distribucija lekova u veterinarskoj medicini
2011
Marković, S., FM PHARM d.o.o., Subotica (Serbia) | Rakovac,V., FM PHARM d.o.o., Subotica (Serbia)
By definition, a veterinary drug is a drug used by veterinarians in the treatment of animal. Due to the large number of animal species and related pathogenic agents, the variety of products manufactured is very wide and the volume of manufacture is often low. The regulation of veterinary medicinal products within the European Union is based on harmonized legislation established at EU. This legislative framework covers the manufacture, authorization (registration), placing on the market and subsequent monitoring of products. The legislation requires a manufacturing authorization certifying that the product is manufactured in compliance with Good Manufacturing Practice (GMP) and a marketing authorization to place the product on the market. The regulation of medicines in the EU is complex and, thereby, flexible in terms of its ability to meet the requirements of stakeholders. The system itself is probably more complex than is appropriate for the actual Serbian situation. Nevertheless, the principles on which the network is based are entirely appropriate for any region considering introducing or enhancing a system for control of medicines.
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