Carmen Jungbäck
IABS-EU, Germany
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Klaus-Peter Behr
Anicon, Germany
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Gerfried Zeller
European Manufacturers of Autogenous Vaccines & Sera (EMAV), Germany
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Peter Schmid
CEVA, Germany
Dušan Palić
Ludwig Maximilian University of Munich, Germany
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Vaughn Kubiak
IABS, France
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Jiři Bures
Institute for State Control of Veterinary Biologicals and Medicines, Czech Republic
Mariette Salery
ANSES-ANMV, France
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Jason Todd
Veterinary Medicines Directorate (VMD), United Kingdom
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Natalie Vasallo
Labocea, France
Maarten De Gussem
Poulpharm, Belgium
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Iska Lehmann
LAVES, Germany
Santiago Cabaleiro
CETGA, Spain
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Max Bastian
FLI, Germany
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Klaus-Peter Behr
EMAV, Germany
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Wiebke Bielenberg
Anicon, Germany
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Rosario Bullido
AEMPS, Spain
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Santiago Cabaleiro
CETGA, Spain
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Panos Christofilogiannis
Aquatreck Animal Health, Greece
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Rory Cooney
VMD, United Kingdom
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Nancy De Briyne
FVE, Belgium
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Maarten De Gussem
Poulpharm, Belgium
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Sebastien Deville
SEPPIC, France
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Laurent Drouet
CEVA, France
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Jean de Foucault
Biovac-CEVA, France
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Ernö Horvath
NEBIH, Hungary
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David John
AHE, Belgium
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Dietmar Katinger
BS-Immun, Austria
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Vaughn Kubiak
IABS, France
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Iska Lehmann
LAVES, Germany
Jordi Lopez
FEADSA, Spain
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Dries Minne
FVE, Belgium
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Petra Mullerova
USKVBL, Czech Republic
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Brigitte Othmar-Vielitz
EMAV , Germany
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Dušan Palić
LMU, Germany
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Dietrich Rassow
FMFA, Germany
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Mariette Salery
ANSES-ANMV, Frace
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Peter Schmid
CEVA, Germany
Alain Schrumpf
CEVA, France
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Ynte Schukken
Royal GD, The Netherlands
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Annie Sigognault-Flochlay
Filavie, France
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Jason Todd
VMD, United Kingdom
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Joris Vandeputte
IABS, Belgium
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Ewald Van Kuppeveld
Ripac, Germany
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Nathalie Vasallo
LABOCEA, France
Gregory Verdier
ANSES-ANMV, France
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Florian Voisin
Hyovet, France
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Gerfried Zeller
EMAV, Germany
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In the process of implementation of REGULATION (EU) 2019/6 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC members of the association of European Manufacturers of Autogenous Vaccines and Sera – EMAV - have compiled common positions for a dedicated GMP Annex for Autogenous vaccines. This proposal defines future standards for the production of Autogenous vaccines to preserve their quality without hindering their manufacturing and availability.

This position paper is an invitation of EMAV to competent authorities, users and other stakeholders to define a new standard for manufacturing and for a secured availability of Autogenous vaccines in the future.

This position paper would become part of the workshop “AUTOGENOUS VACCINES: QUALITY OF PRODUCTION AND MOVEMENT IN A COMMON MARKET”, organized by EMAV and IABS for September 14th – 16th as a hybrid meeting at Munich University LMU too.

The results of the scientific excursus will be incorporated in a IABS – EMAV meeting report and will be shared with all participants of the workshop and all people interested in.

Download the position paper: https://www.emav.be/position-papers

Access to meeting’s slides is given to meeting’s participants for a period of 4 weeks after the meeting.
A unique Login and password are sent by email to participants right after the meeting.
Afterwards the slides are only accessible to IABS member, using their Member Login and Password.


Click here to download the Meeting Slides

This conference is co-organized by the International Alliance for Biological Standardization Europe (IABS-EU) and the European Manufacturers of Autogenous Vaccines & Sera (EMAV).

For further information: