An updated version (v3.0) of the draft guideline on the specifications for provision of an electronic submission (eSubmission) for veterinary medicinal products (Draft VNeeS guideline) is now available. The updates appearing in track-changes have been implemented mostly to align with the VMP-Regulation (EU) 2019/6. Please note that more updates will be envisaged towards October 2021 when relevant guidelines will be published. The basic folder structures as defined in Tables 1 to 3 and Table 6 in this draft guidance are not subject to further change and we would therefore encourage Service providers in charge of updating VNeeS validation tools to use this draft guideline as a basis for updating their systems.
