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

Training courses & Webinars:
Clinical

The objective of clinical studies is to gather the necessary data to ensure the clinical benefits to the animal and to provide the necessary information to comply with the regulations. Our animal health training courses will focus on the clinical requirements for research studies in veterinary medicines, including practical field studies.

 

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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Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight Training Course

Managing Vendor/CRO/CMO Oversight

6-7 Oct 2020 - London
Also on: 8 Oct 2020

Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource

Presented by Laura Brown (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: 29 Oct 2020

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

The New EU Animal Health Legislation for Veterinary Medicinal Products

9-10 Nov 2020 - London
Also on: 11 Nov 2020

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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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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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

Excellent course content with very useful and topical discussions. The speakers were competent and captivating with a good presentation pace.

Kalinka Grozeva, Quality Control Director, Vetagro S.p.A.

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

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