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24-25 June 2020
Radisson Blu Edwardian Grafton,
London

Advanced Regulatory Strategies for Veterinary Drug Development

Accelerate the development of new veterinary pharmaceuticals by understanding how to integrate the European regulatory requirements into a drug development program.

Book with earlybird pricing now!

Receive £100 off if you book before 24 April 2020

COVID-19 UPDATE

We're looking forward to welcoming our attendees and expert course leaders at Advanced Regulatory Strategies for Veterinary Drug Development in London in June.

Our number one priority is the safety of our delegates and colleagues, and there are always measures in place at our venues to safeguard your health and safety. There are extra measures in place for 2020 in light of developments with COVID-19.

Book with total confidence – click here to be fully assured on how your booking rights are protected.

Course Overview

This practical 2-day course has been designed to give you a comprehensive understanding of the EU regulatory requirements that need to be met when developing new veterinary pharmaceutical products.  Over two days you learn how to integrate regulatory affairs with product development, exploring the requirements in key developmental areas such as quality, safety, environmental and efficacy. You will also explore regulatory licensing options available for novel and generic drugs, discussing the specific tests and data required for speedy approval.

What will you learn:

EU regulatory requirements

Understand how to successfully apply the latest EU regulatory requirements to a veterinary drug development program

The regulatory landscape

Gain a deep understanding of the current and future regulatory landscape

How to put theory into practice

Consolidate the theory, with a practical workshop on planning for the development of a new product

Data use and management

Accelerate the regulatory process by understanding what data to use and by learning how to collate it in an effective dossier

Where to find support

Learn how best to seek advice on a novel product development

Dossier submission procedures

Choose the right submission procedure to support your application

Who is this course for?

This course is aimed at professionals who have an active role in the development of new pharmaceutical products. Departments who could benefit include: Regulatory Affairs, Research & Development, Clinical Trials and Marketing. Over two days you will examine the regulatory requirements in key developmental areas providing you the skills to successfully integrate regulatory requirements with the development of new drugs.