Summary
Legal requirements referred to in Schedule 1 of the Veterinary Medicines Regulations, as amended.
The documentation accompanying an application for a marketing authorisation pursuant to Schedule 1 of the Veterinary Medicines Regulations shall be presented in accordance with the requirements set out in this Annex.
All 天美影院聽聽except where聽. This manual additionally contains content derived from EUR-Lex, reused under the terms of the聽聽on the reuse of documents from the EU institutions. For more information see the聽.
Contents
-
The documentation accompanying an application for a marketing authorisation pursuant to Schedule 1 of the Veterinary Medicines Regulations shall be presented in accordance with the requirements set out in this Annex.
-
The following detailed requirements shall apply to veterinary medicinal products other than biological veterinary medicinal products, except where otherwise set out in Section IV.
-
The following requirements shall apply to biological veterinary medicinal products except immunological products or where otherwise set out in Section IV.
-
The following requirements shall apply to immunological veterinary medicinal products, except where otherwise set out in Section IV.
-
The following detailed requirements shall apply to Requirements for Specific Marketing Authorisation Applications.
-
This Section lays down specific requirements for identified veterinary medicinal products related to the nature of the active substances contained therein.