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

In-house & bespoke training:
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

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Tamsin Dawson (bio) , Mel Munro (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

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

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Ruud Bremmers (bio)
and 4 more leading experts

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Advanced Veterinary Pharmacovigilance

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Introduction to Veterinary Pharmacovigilance

In-house & bespoke training

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*

Rated by attendees to the public programme

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Periodic Safety Update Reports for Veterinary Medicinal Products

In-house & bespoke training

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

*NEW EVENT!*

Typically presented by Declan O'Rourke (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Practical Implementation of GCP in Veterinary Field Studies

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Julian Braidwood (bio) , Sue Lester (bio) , Marie-Pascale Tiberghien (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Registration of Animal Feed Additives in the EU

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Joan Castelló (bio) , Elinor McCartney (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Registration of Veterinary Vaccines in the USA and Canada

In-house & bespoke training

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.

Typically presented by Donna Mattson (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

View details

The New EU Animal Health Legislation for Veterinary Medicinal Products

In-house & bespoke training

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*

Rated by attendees to the public programme

Typically presented by Julian Braidwood (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Veterinary Pharmaceutical Submissions in the EU

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Julian Braidwood (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Working Through Veterinary Drug Development in the EU and USA

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Julian Braidwood (bio) , David Petrick (bio)

Typical duration: 5 days
Pricing from £1,500 per attendee
Delivery: collaborative classroom

View details

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

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