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Management Forum

A Practical Approach to Veterinary Vaccine Development and Registration in the EU (European Union) Training Course

This event has been designed to give practical advice and guidance on how to successfully develop market approval in the EU. The programme will take participants through a step-by-step approach to the process and will also provide key guidance on how to maintain MA once achieved.

★★★★★ "Content was great. Presentation and speakers kept me engaged, so very good too. The Interactive Wor... more (21)"

13-14 May 2025
+ 6-7 November 2025 »
from £1099

Need help? Enrol or reserve

Format: Live online
CPD: 12 hours for your records
Certificate of completion

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Course overview

Demand for biologics in veterinary medicine is increasing. However, developing vaccines and successfully obtaining market authorisation brings its own complex and challenging issues.

This course has been designed to give practical advice and guidance on how to successfully develop a veterinary vaccine and achieve market approval in the EU, ensuring that participants gain a comprehensive insight into the necessary requirements.

The programme will take a step-by-step approach to the process and will include a workshop to help delegates gain a better understanding of the requirements in practice. There will be ample time for discussion throughout the two days with our expert faculty and fellow professionals.

Sponsored by:

This course forms part of our selection of Animal Health training courses, designed to keep you up to date with the latest regulations surrounding veterinary medicines, animal feeds, and industry best practices.

Benefits of attending

Recognise the key legislation and guidance and how to use this to plan an effective veterinary vaccine development
Understand what data you need to generate for your application and how to present this in your dossier
Gain an insight into the different routes to market and how to submit your dossier for market approval
Learn how and when to seek regulatory advice during development
Consider the implications of the ongoing review of the Veterinary Medicines Regulations

Who should attend?

This event will be beneficial to all those working with veterinary vaccines from development to market approval.

The programme will be of particular interest to:

New entrants to registration departments
Veterinary medicinal product manufacturers
Registration managers
Research and development departments
Academics with an interest in commercialising opportunities
Personnel from micro/small and medium-sized enterprises (SMEs)

Enrol or reserve

Mel Munro
knoell Animal Health

Dr Mel Munro has worked as a consultant in veterinary medicinal product development and registration for over 20 years. She provides regulatory advice on all areas of biologicals product development taking client projects from proof of concept through to Marketing Authorisation (MA). On a day-to-day basis, she advises on regulatory strategy, performs technical due diligence and gap analyses and prepares strategic development plans and expert reports. She is also experienced in negotiation with the regulators and preparing regulatory documentation. Over her career she has been involved in numerous biologicals projects ranging from more ‘conventional’ vaccines to novel biologicals such as products of rDNA technology, GMO’s, monoclonal antibodies, DNA vaccines and gene therapy.

More details

NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:

30% off the 2nd delegate*
40% off the 3rd delegate*
50% off the 4th delegate*

Please contact us for pricing if you are interested in booking 5 or more delegates

13-14 May 2025

Live online

08:30-15:30 UK (London) (UTC+01)
09:30-16:30 Paris (UTC+02)
03:30-10:30 New York (UTC-04)
Course code 14574

GBP 1,099 1,299
EUR 1,589 1,869
USD 1,817 2,129

Until 08 Apr

2 days live online training
Browser-based, no download usually required
See presenters and interact with fellow attendees
Download documentation and certification of completion
Fair transfer and cancellation policy

View basket

Not ready to book yet?

for 7 days, no obligation

6-7 November 2025

Live online

08:30-15:30 UK (London) (UTC+00)
09:30-16:30 Paris (UTC+01)
03:30-10:30 New York (UTC-05)
Course code 15303

GBP 1,099 1,299
EUR 1,589 1,869
USD 1,817 2,129

Until 02 Oct

2 days live online training
Browser-based, no download usually required
See presenters and interact with fellow attendees
Download documentation and certification of completion
Fair transfer and cancellation policy

View basket

Not ready to book yet?

for 7 days, no obligation

* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.

Reviews of IPI's A Practical Approach to Veterinary Vaccine Development and Registration in the EU training course

Content was great. Presentation and speakers kept me engaged, so very good too. The Interactive Workshop on Product Development was a very helpful exercise

Mar 11 2024

Lillian Sibanda Australia
Assistant Director, Australian Pesticides And Veterinary Medicines Authority

Jul 10 2023

The presentations were clear and precise and a good source for information after the the training.

Gabriele Hoesch Germany
Manager Quality Transfer, Launch & Projects, Boehringer Ingelheim Vetmedica GmbH

Jul 10 2023

It was a very good training regarding all aspects: organisation, speakers, documents, timing. A lot and very useful information.

Yasmina Mallouk France
Quality Assurance Auditor , Boehringer Ingelheim

Mar 17 2022

My intent was to get an overall picture of the lay out of a vaccine registration dossier, content and submission timelines. Thanks to the extensive course, I got a full and complete tool box.

Frédérique Cernicchiaro France
Specialiste Pharmacovigilance Globale, Boehringer Ingelheim

Mar 17 2022

My intent was to get an overall picture of the lay out of a vaccine registration dossier, content and submission timelines. Thanks to the extensive course, I got a full and complete tool box... the webinar has been very enjoyable, informative. Congratulations to both speakers because It is not an easy exercise when addressing attendants through screens.

Frédérique Cernicchiaro France
Specialiste Pharmacovigilance Globale, Boehringer Ingelheim

Mar 17 2022

I think it was especially helpful for the slightly advanced in these areas.

Ladislav Pazout Czech Republic
Production director, DYNTEC, spol. s r. o.

Mar 10 2020

The practical session was very useful, with suitable supporting material for reference, and feedback on interpretation of the monographs

Jonathan Welch United Kingdom
Development Manager (Vaccines), Benchmark Animal Health Ltd

Oct 16 2018

The course was really good, a lot of info packed into two days, but straight forward and logical. The course gave a good overview without going too much into specific details. The workshop was great and really helped a lot for understanding requirements better.

Sebastian Bubendorfer Germany
Scientist, Boehringer Ingelheim Veterinary Research Center GmbH & Co. KG

Oct 16 2018

As you can imagine, the seminar content can be a bit arid for a scientist who is always dealing with lab experiments. Well, I was very surprised by how much the presenters had to share from their vast experience and made sure the course was not only presenting information. They were very dynamic, understood where the questions were coming from and always made sure we got our doubts clarified.

Rocío Leon-Kempis Germany
Head of Bacteriology, Boehringer Ingelheim Veterinary Research Center GmbH & Co. KG

Apr 17 2018

The training was great, it fully met my expectations.

Louise Foster Germany
Regulatory Manager, Semigator GmbH

Apr 17 2018

Interesting and useful.

Eleonora Bastino Belgium
Senior Associate Regulatory Affairs , Zoetis

Oct 16 2018

Good approach to obtain an overview about regulatory affairs. Clear presentations.

Begoña Garcia Monelos Spain
Regulatory Affairs Technician, CZ Veterinaria, S.A.

Oct 18 2017

The speakers were very knowledgeable and provided pertinent suggestions and the course was well presented with a cohesive structure. Content was adequately addressed and explained.

Beverley Taylor United Kingdom
Senior Manager, Regulatory Affairs, Eco Animal Health Ltd

Apr 26 2017

Interesting training, useful for people not only from RA. Documentation complete and helpful.

Anna-Paola Colombo France
Methods Process Improvement Specialist, Merial SAS

Apr 26 2017

The course was excellent in so far as it was tailored to individual needs and requirements. The materials provided are invaluable; they will help me with future projects. Overall a thoroughly enjoyable and useful training course.

Callum Scott United Kingdom
Vaccine Development Manager, Benchmark Animal Health Ltd

Apr 26 2017

I am satisfied!

Ágnes Bárdi Hungary
Registration Expert, Ceva - Phylaxia Veterinary Biologicals co. Ltd.

Apr 26 2017

Great course. Would recommend. I appreciate that it is narrowed down to veterinary vaccine development in the EU. Most other courses I have come across covers many RA topics at once but this was more targeted. Even so, there was plenty of material to go through and we could get a bit more in depth.

Matias Nilsson Denmark
Regulatory Affairs Specialist & QPPV, Salfarm Danmark A/S