Regulatory Services

The requirement to register a company and product with a 

reference body to approve their registration in the state 

 

 

We would like to inform you that this decision of the Superior Committee for the registration of veterinary medicines in the State Council No. 4/2016 on 8/12/2016 

Which was directed not to accept the receipt of files of companies and products not registered with at least one reference body , which was  determined according to the following : 

 

United States of America - Canada - Australia - Japan

   European Medicines Authority

(Belgium - Denmark - Germany - Spain - France - Ireland - Italy - Lithuania - Hungary - Netherlands - Austria - Romania - Finland - Sweden - Switzerland - New Zealand - Britain - Norway - Romania-Czech Republic - Estonia - Bulgaria - Greece - Croatia - Cyprus - Latvia - Luxembourg - Malta - Poland - Norway - Slovenia - Slovak Republic )

 

Turkey - Saudi Arabia - Kuwait - South Africa …