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Informa Life Sciences

Regulation of Veterinary Medicines in Europe 2008

  
   

Regulation of Veterinary Medicines in Europe 2008
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Tue 04 Mar 2008 - Wed 05 Mar 2008
Radisson SAS Royal Hotel, Dublin, Ireland (Republic of)

Informa Life Sciences' 4th Annual 'Regulation of Veterinary Medicines in Europe 2008' is the premier forum for the discussion of Animal Health regulatory issues. This year the conference has a new expanded format including a dedicated track for the registration of generic products. Addressing all aspects of regulation, this conference provides excellent choice and networking opportunities giving delegates the opportunity to move between streams.

 

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Who Will Attend?

This is the must attend conference of 2008 for all:

Registration Managers, Regulatory Affairs Managers, Global Directors, Head of Animal Health Product Development, Regional Technical Managers, Regulatory Affairs Directors, Regulatory Affairs Excutives, Managing Directors and CEOs



Don't Miss

 

Meet the European regulators and learn from the experience of renowned experts. If you attend one conference next year make it ‘Regulation of Veterinary Medicines 2008’ and gain:

-         Up-to-the-minute information on amendments to pharmacovigilance, safety and the recasting of variations legislation

-         Advice and guidance on the environmental impact assessment for R&D and generic submissions

-         Practical experience from the new pharmacovigilance inspections

-         Opportunities to put your questions to the regulators in interactive panel sessions

-         Tips and advice for your on and off patent products

-         Real industry examples of dossier production, DCP submissions, efficacy and safety studies

-         A look at the availability of medicines and MUMS

-         Excellent networking opportunities in the form of scheduled networking breaks and speed-networking sessions

-         Choice over the sessions which YOU want to attend

And much much more!

Animal Pharm


Who Will You Meet

- Emma Soto, Policy Officer, DG SANCO, Health and Consumer Protection Directorate General, European Commission, Belgium

- Cornelia Ibrahim, Head of Department, Support and Surveillance after Authorisation, The Federal Office of Consumer Protection and Food Safety (BVL), Germany

- Gabriel Beechinor, Director of Veterinary Medicines, Irish Medicines Board (IMB), Republic of Ireland

- Jackie Atkinson, Director, Authorisations Division, Veterinary Medicines Directorate (VMD), UK

- Gaël Virlouvet, Rapporteur for National and European Procedures, Chemicals Unit, National Agency for Veterinary Medicinal (AFSSA), France

- Michèle Dagorn, Head of the Pharmacovigilance Unit, National Agency for Veterinary Medicinal Products (AFSSA), France

- Joop de Knecht, Senior Assessor, National Institute for Public Health and the Environment (RIVM), The Netherlands

- Asbjørn Brandt, Head of the Department of Veterinary Medicines, Medicines Agency, Denmark

- Karolina Törneke, Senior Expert, Medical Products Agency, Sweden

- Helena Ponte, Head of Division, Management and Evaluation of Veterinary Medicines and Products, Ministry of Agriculture and Former president of Council Working Party of Veterinary Experts in Public Health for the amendment of Reg. 2377/90, Portugal

- Tonje Høy, Head of Section for Veterinary Medicine Licensing Department, Medicines Agency, Norway

- Lesley Johnson, Head of Pharmaceuticals and Feed Additives, VMD, UK

- A Representative from The European Food Safety Authority (EFSA), Italy

- Jiri Bures, Project Manager, Institute for State Control of Veterinary Biologicals & Medicaments, Czech Republic

 

- Dr Lillian Cromie, Head of Research and Development, Norbrook Laboratories Ltd, Northern Ireland 

- Rob Jooston, Head of Regulatory Affairs and Development, Eurovet Animal Health BV, The Netherlands

- Cait Brennan, Veterinary Regulatory Affairs Manager, Channelle Pharmaceuticals Manufacturing Ltd., Republic of Ireland

- Bert Sorenen, Global Regulatory Affairs Director, HUVEPHARMA NV, Belgium

- Olivier Roy, Head of Preclinical and Clinical Veterinary Department, CEBIPHAR, France

- Katie Barrett, Programme Director and Scientific Manager, Ecotoxicology, Huntingdon Life Sciences, UK

- Dr Xavier Pineau, Vice Head of Veterinary Pharmacovigilance, Centre of Lyon, France

- Elisabethann Wright, Counsel, Hogan & Hartson LLP, Belgium

- Noël J. Akers, Chartered Patent Attorney, N.J. Akers & Co., European Patent and Trade Mark Attorneys, UK

- Hector Armengod, Associate, Hogan & Hartson LLP, Belgium

- Marjan Noor, Taylor Wessing, UK

 



Group Discounts
For more info call:
Simon Lau
Tel: +44 (0) 20 7017 7165
Email:simon.lau@informa.com
Speaker Opportunities
To discuss opportunities call:
Gemma Cook
Tel: +44 (0) 20 7017 5880
Email:gemma.cook@informa.com
Sponsorship and Exhibition
To discuss opportunities call:
Martin Cheung
Tel: +44 (0) 20 7017 4938
Email:martin.cheung@informa.com