This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Starting TBC
LIVE Online Academy
Starting TBC

LIVE Online Academy

Understand the regulations surrounding the authorisation and maintenance of veterinary medicinal products in the EU

Course Overview

Veterinary medicines follow a strict regulatory framework to ensure the wellbeing of animals and to keep animals healthy in the food chain for human consumption.

This course is designed for the regulatory professional to give a complete guide to the regulatory guidelines surrounding the authorisation of veterinary medicinal products in the EU. The course will provide you with fundamental regulatory knowledge to help you unpick the complexity of the system and apply your knowledge to achieve fast product approval and effective product maintenance.

You will explore the regulatory landscape for veterinary medicines and examine the European licensing procedure for product approval. You will discuss in detail the submission process, analysing areas such as quality and efficacy.

Live Online Academies

Gain real-time access to a subject matter expert delivering online training in a structured virtual classroom environment. Live online academies are virtual versions of some of our most popular face-to-face courses.

Students will learn through:

  • Live interactive sessions
  • Direct interaction with the trainer during live sessions
  • Participation in interactive features within sessions including polls, Q&A, break out rooms, tasks, case studies, and more
  • Revisiting recorded sessions with unlimited access for 30 days
  • Interaction with peers during live sessions and through the online forum

Timings and dates are subject to change - final confirmation will be provided with login details. Delegates will receive login instructions within a week of the course start date. If you have any questions please contact

What will you learn?

Regulatory developments

Understand and successfully apply the latest directive to your marketing authorisations

Submission procedures

Choose the right submission procedure to support your application


Establish your veterinary pharmacovigilance reporting systems

Packaging & Labelling

Comply with the latest regulations for packaging and labelling of veterinary medicinal products


Learn how to maintain your marketing authorisation with a practical guide to variations

Who is this course for?

This course has been specifically designed for those working in the development of new veterinary medicinal products

  • Regulatory Affairs
  • Document Management
  • Project Managers in Regulatory Affairs
  • Research & Development

CPD Certified

Engaging in Continuing Professional Development ensures that both academic and practical qualifications do not become out-dated or obsolete; allowing individuals to continually ‘up skill’ or ‘re-skill’ themselves, regardless of occupation, age or educational level. This course has been assessed and is CPD certified.

Clinical R&D


Boehringer Ingelheim

The course definitely covered my needs. It was interactive and provided additional information.

Delegates of our live online academies said...


would attend another live online academy


found the course beneficial to their day to day role


would recommend the course to others