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Animal Health

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.

Book by 26 Jan to save
£200 / €280 / $312

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

Book by 22 Oct to save
£200 / €280 / $312

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

Advanced Veterinary Pharmacovigilance

25-26 Nov 2020

Also on: 23 Jun 2021

Book by 14 Oct to save
£200 / €280 / $312

Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.

Effective Technical Writing & Editing

24 Sep 2020

Also on: 11 Feb 2021

Book by 13 Aug to save
£100 / €140 / $156

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

3 Dec 2020

Also on: 28 Jun 2021

Book by 22 Oct to save
£100 / €140 / $156

This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA.

Book by 23 Oct to save
£100 / €140 / $156

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*

Introduction to Veterinary Pharmacovigilance

14-15 Oct 2020

Also on: 20 Apr 2021

Book by 2 Sep to save
£200 / €280 / $312

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

Managing Vendor/CRO/CMO Oversight

8-9 Oct 2020

Also on: 26 Apr 2021

Book by 27 Aug to save
£200 / €280 / $312

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

*NEW EVENT!*

Book by 23 Sep to save
£200 / €280 / $312

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.

Book by 15 Sep to save
£200 / €280 / $312

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

Book by 5 May to save
£200 / €280 / $312

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.

Book by 28 Jan to save
£100 / €140 / $156

Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.

Successful Medical Writing

5-7 Oct 2020

Also on: 24 May 2021

Book by 24 Aug to save
£300 / €420 / $468

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*

Book by 30 Sep to save
£200 / €280 / $312

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

18-19 Nov 2020

Also on: 16 Mar 2021

Book by 7 Oct to save
£200 / €280 / $312

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

Book by 26 Apr to save
£400 / €560 / $624