Our latest COVID-19 information - full Autumn programme of webinars now in place

Training courses & Webinars:
Regulatory

Veterinary pharmacovigilance is the on-going monitoring of the safety and efficacy of medicines used for the prevention, diagnosis and treatment of disease in animals. Our pharmacovigilance training courses will provide participants with the necessary information to comply with latest regulations.

 

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

A Practical Approach to Veterinary Vaccine Development and Registration in the EU

9-10 Mar 2021 - Online webinar
Also on: 11 Mar 2021

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.

Presented by Tamsin Dawson (bio)
Mel Munro (bio)

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A Regulatory Update on Animal Feed and Feed Additives in the EU (European Union), USA and China Training Course

A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China

3-4 Dec 2020 - Online webinar
Also on: 2 Dec 2021

Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China – now in its tenth successful year.

Presented by Ruud Bremmers (bio)
and 4 more leading experts

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Advanced Veterinary Pharmacovigilance Training Course

Advanced Veterinary Pharmacovigilance

25-26 Nov 2020 - Online webinar
Also on: 21 Jun 2021

Including the main requirements of Volume IXB, an update on the proposed EU Regulation (2019/6) on Veterinary Medicinal Products and the impact of Brexit

Presented by Declan O'Rourke (bio)

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Introduction to Veterinary Pharmacovigilance Training Course

Introduction to Veterinary Pharmacovigilance

14-15 Oct 2020 - Online webinar
Also on: 20 Apr 2021

A basic training course for those working on drug safety in the EU. This course has been designed to provide basic training and a good introduction to those concerned with veterinary pharmacovigilance.

*INCLUDES: Interactive workshop and discussion sessions*

Presented by Declan O'Rourke (bio)

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Periodic Safety Update Reports for Veterinary Medicinal Products Training Course

Periodic Safety Update Reports for Veterinary Medicinal Products

4-5 Nov 2020 - Online webinar
Also on: 11 May 2021

Including requirements for regions including the EEA, USA, Canada and Australia and an update on the implications of Brexit

*NEW EVENT!*

Presented by Declan O'Rourke (bio)

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Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course

Practical Implementation of GCP in Veterinary Field Studies

27-28 Oct 2020 - Online webinar
Also on: 27 Apr 2021

This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with Good Clinical Practice (GCP) as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP.

Presented by Julian Braidwood (bio)
Sue Lester (bio)
Marie-Pascale Tiberghien (bio)

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Registration of Animal Feed Additives in the EU (European Union) Training Course

Registration of Animal Feed Additives in the EU

14-15 Jun 2021 - London
Also on: 16 Jun 2021

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

Presented by Joan Castelló (bio)
Elinor McCartney (bio)

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Registration of Veterinary Vaccines in the USA and Canada Training Course

Registration of Veterinary Vaccines in the USA and Canada

11 Mar 2021 - Online webinar
Also on: 12 Mar 2021

This course will cover some of the most complex yet fundamental aspects of veterinary vaccines licensing by USDA and CFIA including the phased submission process as well as the format and content specifications for the required dossier components.

Presented by Donna Mattson (bio)

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The New EU (European Union) Animal Health Legislation for Veterinary Medicinal Products Training Course

The New EU Animal Health Legislation for Veterinary Medicinal Products

11-12 Nov 2020 - Online webinar
Also on: 5 May 2021

The programme will offer a comprehensive introduction to the new EU Regulation (2019/6) and will address the changes and implications to the industry including marketing authorisations, submissions and dossiers.

*INCLUDES: Interactive discussion sessions*

Presented by Julian Braidwood (bio)

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Veterinary Pharmaceutical Submissions in the EU (European Union) Training Course

Veterinary Pharmaceutical Submissions in the EU

18-19 Nov 2020 - Online webinar
Also on: 16 Mar 2021

Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, detailed and critical summaries and regulatory submissions.

Presented by Julian Braidwood (bio)

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Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course

Working Through Veterinary Drug Development in the EU and USA

7-10 Jun 2021 - London

This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.

Presented by Julian Braidwood (bio)
David Petrick (bio)

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I really enjoyed this course. The interactions with other participants and the flexibility of the speaker to engage in real-world scenarios helped to put the course content into perspective. It was nice to know that other companies face similar challenges, and get practical solutions and advice from the speaker.

Amanda Dwyer, Pharmacovigilance Manager, North America, Elanco Animal Heallth

The main themes of the new Regulation were presented in a precise but detailed manner and this, coupled with the extensive knowledge and sympathetic manner of the speaker, make the course something special.

Heike Luckow, Regulatory Affairs, Bela-Pharm GmbH & Co. KG

All speakers delivered their presentations in a clear and concise manner, supported by informative slides.

Beccy Christmas, Regulatory Affairs Officer, Micron Bio-Systems Ltd

My goal was to gain an overall understanding of registrations in China and USA and I succeeded in that, thanks to the speakers who were excellent.

Rosa Vainio, Product Registration Specialist, Hankkija Oy

Well-organised course with the relevant content I needed to stay on top of the field and a good opportunity to meet other professionals. I very much appreciated having the printed presentations as it makes taking notes much more efficient.

Adalberto Costessi, Product Manager, BaseClear

An interesting, informative and interactive two-day course which provided a clear overview and explanation of the most important changes that we can expect as a result of the 2019/6 Legislation. It is not easy to keep the audience interested while explaining a new law but Julian managed to do this excellently.

Kitty Ruigrok, DVM, Regivet BV

All good and informative.

Helena Oliveira, Regulatory Affairs Manager, Nutreco Nederland BV

Hector's presentation was the clearest analysis I have seen on the effects of Brexit on UK industry and the economy.

David Pickard, Regulatory Manager, Inroads International Ltd

As with previous years the course was very informative and gave a rounded set of opinions from various perspectives (industry, EFSA, consultants etc).

Joshua Forster, Regulatory Executive, CYTON BIOSCIENCES LTD

Very well presented, very informative content and a friendly atmosphere.

Maria Brogan, Formulation Technologist Manager, Mervue Laboratory