Examples of Veterinary Use in a sentence
EudraLex Volume 4 Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use.
Amount EUR 41 000Description and objective of the implementing measure The purpose of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Veterinary Use (VICH) is to bring together the drug regulatory authorities of EU, Japan and the United States along with experts from the pharmaceutical industry in the three regions to discuss scientific and technical aspects of product registration.
Assessments and authorisation decisions are made by the Committee for Medicinal Products for Veterinary Use (http://www.emea.europa.eu/htms/general/contacts/CVMP/CVMP.html).
Exemptions and reductions are granted on fees relating to applications for products classified by the Committee for Medicinal Products for Veterinary Use (CVMP) as indicated for minor use minor species and for which the market is confirmed by the Committee as 'limited'.The fee incentives are applicable for as long as the product concerned remains classified by the Committee as (a) MUMS/limited market and (b) eligible for fee incentives.
Amount EUR 42 000Description and objective of the implementing measure The purpose of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Veterinary Use (VICH) (52) is to bring together the drug regulatory authorities of EU, Japan and the United States along with experts from the pharmaceutical industry in the three regions to discuss scientific and technical aspects of product registration.
With respect to Veterinary Use, unless set forth in a separate written agreement between the Parties, no research, development or commercialization costs and expenses are intended to be shared by the Parties and no milestones or royalties set forth herein shall apply to the Development or Commercialization of any Optioned Product for Veterinary Use.
Manufacturing Practice for Medicinal Products for Human and Veterinary Use, Chapter 1, Pharmaceutical Quality System.
In the case of medicinal products whose marketing authorisation in the EU is submitted via the centralised procedure, when the Committee for Medicinal Products for Veterinary Use (CVMP) requests Anses-ANMV for an inspection of the manufacturing facilities of that medicinal product, an inspection announcement letter shall be sent by the EMA to the holder of that medicinal product.
Article 114 of Directive 2001/83/EC as amended by Directive 2004/27/EC is transposed in the Belgian legislation in the Royal Decree of 14/12/2006 related to the Medicinal Products for Human and Veterinary Use (published the 22/12/2006 in the Belgian official journal).Article 89 describes the principle of batch release for the immunological products.In conformity with the EU directive we perform the batch release testing on vaccines batches for the European market.
URL https://doi.org/10.1038/476393a.ECDC and EFSA Panel on Biological Hazards (BIOHAZ) and EMA Committee for Medici- nal Products for Veterinary Use (CVMP).