Animal Health

This meeting 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.

Two day meeting on Regulation Update on Animal Feed and Feed Additives in the EU, USA and China, annual conference now in its 6th successful year.

Advanced Veterinary Pharmacovigilance – the purpose of this course is to provide a comprehensive, yet practical assessment of the main requirements to ensure a compliant reporting Company.

Advanced Veterinary Pharmacovigilance

21-22 Mar 2018

Also on: 2 Oct 2018

A practical five day In-house course Working through Veterinary Drug Development in the EU and the USA

An essential course for ensuring compliance with Regulatory Requirements which will be of particular relevance for Pharmacovigilance, Regulatory Affairs, Clinical Research/Operations, GMP, QA and Document Management Functions

How to Write Effective SOPs

6 Dec 2017

Also on: 28 Jun 2018

A basic In-house 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.

Introduction to Veterinary Pharmacovigilance

2-3 May 2018

Also on: 7 Nov 2018

This comprehensive two day course will introduce you to the core concepts of what makes an excellent leader – in the context of the pharmaceutical industry – and how to apply the different skills of leading your staff and team to maximise results

Leadership Skills for Pharmaceutical Professionals

21-22 Jun 2018

Also on: 26 Nov 2018

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.

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 GCP as outlined in the two guidelines on safety and efficacy produced by FEDESA and CVMP.

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

Understand the licensing of veterinary vaccines by USDA and CFIA, understand the phased submission process for vaccine licensing, and learn the format and content specifications for the required dossier components.

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

Veterinary Pharmaceutical Submissions in the EU

28-29 Nov 2017

Also on: 25 Apr 2018