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All comments can be sent at [email protected]. Deadline of submission of comments shall be by 31 March 2021


Republic Act No. 9711 otherwise known as the “Food and Drug Administration Act of 2009”, as enacted by the congress on 18 August 2009, among others, has the objective of strengthening and enhancing the administrative and technical capacity of the Food and Drug Administration (FDA) through the regulation and monitoring of establishments and products under its mandate, which include veterinary drugs & products.

To maintain the effectiveness of the regulation of the veterinary drugs products, ensure efficient supply thereof, and strengthen public protection to emerging health concerns such as antimicrobial resistance, the following guidelines are set forth herein.

Read more:-> Draft Revised Guidelines on the Licensing of Veterinary Establishments, Registration and Post-Market Surveillance of Veterinary Drug Products