Animal Health

VETERINARY EXPERT REPORT
24 February
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This seminar aims to provide guidance for those concerned with the preparation of veterinary pharmaceutical and immunological product registration dossiers in the EU. Requirements under EU legislation will be covered, including those of Regulations 2309/93 (Centralised Procedure) and 2377/90 (MRLS) as well as Directive 81/851 (National and Decentralised Procedures). The requirements for Expert Reports as part of the dossier for feed additives (Directive 70/524) will also be included.
Conference No N2-8505
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THE REGULATION OF VETERINARY MEDICINAL PRODUCTS IN EUROPE
9 & 10 March
Keynote address: STEVE DEAN, Director & CEO, Veterinary Medicines Directorate, UK 
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Following completion of the codification process, the new regulatory framework for veterinary medicines in Europe is now at an advanced stage of development in the institutions of the European Union. This major international conference will examine the new legislation, as well as reviewing critical issues in the implementation of current requirements. The other major issue confronting both industry and regulators is the integration of the accession countries into an enlarged European Union. The impact of this major step forward will be reviewed in detail. This conference provides an opportunity for anyone working in government or industry to hear an up to date assessment of the European regulatory situation concerning veterinary medicines by a number of distinguished representatives from both regulatory authorities and industry
Conference No V3-8005
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BIOTECHNOLOGY FOR THE NON-BIOTECHNOLOGIST
10/11 March
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Conference No M3-6405
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ANIMAL FEED ADDITIVES SUBMISSIONS
17 March
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Successful EU feed applications require a significant financial investment and dossiers take 2 to 5 years for completion. Forward thinking companies are now planning their EU feed additive registration projects.This seminar will provide guidance on the production of feed additive dossiers and how to prepare successful applications.
Conference No V3-8205
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The Animal Health Summer School
WORKING THROUGH VETERINARY DRUG DEVELOPMENT
6-10 June
This course has been designed to demonstrate how pharmaceutical, pharmacological, toxicological and clinical investigations and regulatory management are brought together in the development programme. It will take the participants through all of the stages in the development of a veterinary medicinal product for which a marketing authorisation is sought in the European Union. Presentations will cover pharmaceutical and process development, toxicological, pharmacological, residues and ecotoxicological studies, safety risk assessments, clinical development, regulatory and marketing input and project management. An important part of the course will be devoted to working on case studies in the workshop sessions. The course will provide a comprehensive introduction to the entire development programme.
Conference No V6-8005
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BIOTECHNOLOGY FOR THE NON-BIOTECHNOLOGIST
29/30 September
Conference No M9-6005
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If you have any suggestions for further meetings please contact Andrea James
Tel: +44(0)1483 570099